对硝基甲苯合成对氨基苯甲酸实验报告.docx
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对硝基甲苯合成对氨基苯甲酸实验报告.docx
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对硝基甲苯合成对氨基苯甲酸实验报告
武汉大学化学与分子科学学院
有机化学实验报告
实验名称:
synthesisof4-aminobenzoicacidfrom4-nitrotoluene
班级:
化学弘毅班姓名:
指导老师:
熊英
实验日期:
5.11-6.8星期:
四实验室:
化东514
一.目的要求:
1.Reviewthefundamentaloperationsoforganicexperiment,suchassimpledistillation,recrystallizationandthedeterminationofmeltingpoint.
2.Befamiliarwithphysicochemicalpropertiesofthereagentsandlearntodesigntheproceduresaccordingtoreferencestoobtain4-aminobenzoicacidfrom4-nitrotoluene.
3.DeterminetheproductsofeverystepbyTLC,IR,meltingpointdeterminationor1HNMR,andlearntoanalyzetheresultstotestifytheefficiencyandthevalidityoftheexperiments.
二.反应原理:
Thechemicalreactionsareshowedinthefollowing:
Aromaticcarboxylicacidsareoftenpreparedbyoxidationofaromaticsidechains.Thearomaticringofaromatichydrocarbonsisrelativelystableanddifficulttooxidize,andthechainoftheringregardlessoflength,aslongasithasα-H,inthestrongoxidation,itwillfinallybeoxidizedtocarboxylgroups.Thelaboratorygenerallyoxidizestoluenebypotassiumpermanganatetoproducebenzoicacid
Sincetolueneisinsolubleinpotassiumpermanganateaqueoussolution,thereactionisatwo-phasereaction,sothereactionneedstobesufficientlystirredandrefluxedatahighertemperatureforarelativelylongperiodoftime.Afterheatingandrefluxing,thepotassiumsaltofthebenzoicacidandtheprecipitationofmanganesedioxideareobtainedinthefirstplace.Theprecipitateisseparatedandthepotassiumsaltofthebenzoicacidisacidifiedwithhydrochloricacidtoobtainbenzoicacid,whichishardlysolubleinwaterandcrystallizedeasily.
ThereductionofnitrogroupcanbedonebyFepowderwithacetateorSnpowderwithcondensedHCl.Feismuchcheaperbuttheyieldislower,sowechoosetouseSnasreductant.Asamatteroffact,theSnsaltofaminobenzoicacidistoxicandneedsspecialcaretopreventskinexposureandinhalation.
三.主要试剂及产物的物理常数:
名称
分子量
性状
折光率
比重
熔点(oC)
沸点(oC)
溶解度(克/100ml溶剂)
水
醇
醚
4-nitrotoluene
137.1378
Yellowobliquefacadecrystal
1.5382
1.29
51.7
238.5
insoluble
Readilysoluble
Readilysoluble
4-nitrobenzoicacid
167.13
Yelloworwhiteobliquefacadecrystal
unknown
1.610
239~241
unknown
<0.1g
soluble
soluble
4-aminobenzoicacid
137.14
Colorlessneedle-likecrystal
1.374(25℃)
187~187.5
unknown
Readilysoluble(hot)
sparinglysoluble(cold)
Readilysoluble
Readilysoluble
四.主要试剂用量及规格:
试剂名称
用量
规格
试剂名称
用量
规格
4-nitrotoluene
2.5g
A.R.
ligroin
20ml
60-90oC
Potassiumpermanganate
12.5g
A.R.
NaOH(aq)
20ml
50%
Sulfuricacid
7.5ml
condensed
Ethylacetate
20ml
A.R.
Sn
4g
powder
ammoniawater
30ml
condensed
Hydrochloricacid
15ml
condensed
cyclohexane
30ml
A.R.
ethanol
20ml
A.R.
五.实验装置图:
六.时间表
Time
synthesis
characterization
WEEK1
Oxidationof4-nitrotoluene
WEEK2
Purification
m.p.determination,TLC
IR
WEEK3
Reductionof4-nitrobenzoicacid
WEEK4
Purification
H-NMR
WEEK5
IR
七.实验步骤及现象:
Thefirstweek:
oxidationofp-nitrotoluene
1.Preparationofcrudeproduct
Placethemagnetina100mlroundbottomflask,andadd2.5g(0.02mol)ofp-nitrotolueneand30mLofwater,chargetherefluxcondenser,stirandheattoreflux.Add6.00g(0.04mol)ofpotassiumpermanganateinportionsfromthemouthofthecondensertubewithin30minutes.Incaseofpotassiumpermanganatepluggingthecondenser,asmallamountofwatercanbeusedtorinsetheinnerwallofthecondensertube.Afterthat,plusasmallamountofwatertowashthepotassiumpermanganateattachedtotheinnerwallofthecondenserintothebottle,thetotalwatershouldnotexceed10mL.Continuerefluxuntilthetoluenelargelydisappears.Keeprefluxformorethan60minaftertheadditionofpotassiumpermanganate.
2.Crudeproductseparation
PumpthemixtureintheroundbottomflaskunderreducedpressurewithawaterpumpandwashtheMnO2residuewithasmallamountofhotwater.Ifthefiltrateispurple,addasmallamountofsaturatedsodiumbisulfitesolutiontomakethecolordisappear,andre-filter.Pourthefiltrateintoabeakerandplaceinanice-waterbath,coolandacidifywithconcentratedhydrochloricaciduntilallp-nitrobenzoicacidisprecipitated.Filtertheprecipitatedp-nitrobenzoicacidunderreducedpressure,washitwithasmallamountoficewater,andthendryittoobtaincrudeproduct.
Thesecondweek:
purificationandcharacterizationofp-nitrobenzoicacid
3.Productrefinement
Afterdrying,recrystallizedthecrudeproductinwater.Aftertheproductisdried,weighitandcalculatetheyield.
4.characterization
DoTLCanalysesofbothcrudeandpurifiedproduct,meltingpointdeterminationofbothcrudeandpurifiedproduct,IRdeterminationofpurifiedproduct.
Thethirdweek:
reductionofp-nitrobenzoicacid
5.Preparationofcrudeproduct
Placethemagnetina50mlthree-neckedflask,thenadd4g(0.025mol)ofSnpowder,2.00g(0.012mol)ofp-nitrobenzoicacidproductand5mlofwatertothemouth.Thenadd3.5ml(about0.04mol)ofconcentratedhydrochloricaciddropwisetothereactionsystem.Duringtheadditionofconcentratedhydrochloricacid,keepthemagnetspinning.Whentheadditioniscompleted,keepheatingtorefluxuntilthereactioniscompleted.
6.Crudeproductseparation
Coolingthesystem,thenadd50%sodiumhydroxidesolutiontothesystemisalkaline.Slowlyadddilutehydrochloricacid,precipitationofsolidwillappearintheicebath.Filterthecrudeproductunderreducedpressure.
Thefourthweek:
Recrystallizationofp-aminobenzoicacid
7.Productrefinement
Dissolvethecrudeproductwithasmallamountofethanolwithheating,andthenaddpetroleumether.Coolthesolutionandsolidprecipitates.
DoH-NMRdetermination.
Thefifthweek:
IRdeterminationandcleaningtheapparatus
8.characerizationandendoftheexperiment
DoIRdeterminationofthefinalproductandcleanandchecktheapparatuses.
Thepotassiumpermanganatewascrushedbyaglassstopper,andthenaddedintotheflaskin3timesin30minutes.(1:
40-14:
05)
Thepluginthecondenserblockoccurredinthesecondaddition.
Thesolutionturnedpurpleaftertheaddition,andsomebrownsubstanceclungtotheinnersurfaceoftheflask.Aftershaking,itgraduallydissolvedintothesolution.
Smallamountofsodiumbisulfitesolutionwasadded,andthesolutionfainted.
Relux(14:
05-15:
06)
0.85glightyellowsubsidencewascollected.
Thesubsidencewasaddedintoaround20mlwater,thenNaOHsolutionwasaddedtomakethesoliddissolve.Thesolutionbecamelightyellow.Byadditionofdilutehydrochloricacid,subsidenceappearedinicebath.
0.73gofrefinedgrayishyellowproductwasobtained.
Becausetheproductdidnotreachexpectedamount,otherchemicalswasmodifiedaccordingly.
Thedosage:
p-nitrobenzoicacid:
0.70g
Snpowder:
2.18g
H2O:
4ml
concentratedhydrochloricacid:
2.5ml
Thesolutionwasyellow.
TherestillremainedsomeSnpowderwhichwasseparatedbyfiltering.
Duringtheadditionofsodiumhydroxide,aseriesofphenomenonappeared:
thesolutionbecamewhiteandstickyatfirst(itwasstillacidic),thenitbecamewhitesolution,afterthatthesolutionbecameclear(itwasalkaline,pH=11).
Afterfiltratingoutthesubsidence,dilutehydrochloricacidwasadded.Inthefirstplace,somegrainlikesubsidenceshowedup,thenitbecameturbid.
0.9020gcrudeproductwasgainedafterfiltrationanddrying.
Assoonaspetroleumetherwasadded,whitesubsidenceappeared.
0.1103grefinedproductwasgainedafterfiltrationanddrying.
八.数据记录表格:
Theoxidationprocedure:
Theweightofcrudep-nitrobenzoicacid:
0.85g
Theweightofpurifiedp-nitrobenzoicacid:
0.73g
TLCanalyses:
Product(crude)p-nitrotolueneProduct(purfied)p-nitrotoluene
Rf=0.18Rf=0.87Rf=0.17Rf=0.89
m.p.determination(crudeproduct)
Tfirst
Ttot
ΔT
T
Taverage
1
234
239
5
236
237
2
235
239
4
237
m.p.determination(refinedproduct)
Tfirst
Ttot
ΔT
T
Taverage
1
237
240
3
238
239
2
237
241
4
239
Thereductionprocedure:
Theweightofcrudep-aminobenzoicacid:
0.9020g
Theweightofrecrystallizedp-aminobenzoicacid:
0.1103g
九.产率计算:
Theyieldofp-nitrobenzoicacid:
0.73g÷167.13g/mol÷(2.5g÷137.1378g/mol)×100%=23.96%
Theyieldofp-aminobenzoicacid:
0.1103g÷137.14g/mol÷(0.73g÷167.13g/mol)×100%=18.41%
Totalyield:
23.96%×18.41%=4.41%
十.实验讨论:
Theyieldwasrelativelylow,anddidnotreachthereportedyieldaccordingtothereferences.Thefollowingreasonsmaygivetheexplanations:
1.Because250mlthree-neckedflaskwasnotoffered,theamountofingredientcouldnotmatchwhathadbeenrequiredintheexperimentalscheme.Theamountofingredientwashalved,whichmeanttheregularlossintransferandotherexperimentaloperationsaccountedformoreproportion.
2.Intheoxidationprocedure,thetimeforrefluxwas60min,whichseemednotlongenoughforp-nitrotoluenetobecompletelyoxidized.
3.TherewasnoneedtodothepurificationinthesecondweeksinceTLCanalysisshowedtheproductdidnotcontaintheingredient--p-nitrotoluene.Andrecrystallizationinevitablyreducedtheyieldofp-nitrobenzoicacid.
4.Althoughpetroleumloweredp-aminobenzoicacid’ssolubilityinethanol,therestilldissolvedarelativelargeamountofproductinthesolvent.
5.ThepHwasnotsetwellwhencrudep-aminobenzo
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- 硝基 甲苯 合成 氨基 苯甲酸 实验 报告