4-Nitrobenzoic Acid → Phenylmethyl 4-nitrobenzoate

HRID 467800

반응식

HRID 467800 반응식
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].C(=O)([O-])[O-].[K+].[K+].[CH2:19](Br)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>CC#N>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:8]([O:10][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:9])=[CH:11][CH:12]=1)([O-:3])=[O:2]

참가 물질

5

반응물 3

HCID 61084-Nitrobenzoic AcidHCID 7498Benzyl BromideHCID 11430Potassium Carbonate

생성물 1

HCID 84647Phenylmethyl 4-nitrobenzoate수율 89.1%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

15.01 g (89.9 mmol) 4-nitrobenzoic acid are suspended in 500 mL MeCN and then combined with 15.03 g (108.7 mmol, 1.2 eq) potassium carbonate. 15.4 g (90.4 mmol, 1.01 eq) benzylbromide are added dropwise with stirring and the reaction mixture is heated for 5 h with stirring at 60° C. It is combined with 750 mL distilled water, extracted 4 times with 250 mL of EE and after the organic phases have been combined dried on sodium sulphate. After all the volatile constituents have been eliminated in vacuo the crude product is suspended twice in succession in toluene and evaporated down in vacuo. 20.6 g (80.1 mmol) benzyl 4-nitrobenzoate are obtained, which is used in the next step without any further purification.

후처리

  1. temperaturethe reaction mixture is heated for 5 h
  2. stirringwith stirring at 60° C
  3. distillationdistilled water
  4. extractionextracted 4 times with 250 mL of EE
  5. customafter the organic phases have been combined dried on sodium sulphate
  6. customevaporated down in vacuo

출처 및 근거

ORD 기록
ord-f4c430d1f18b4c93a9736d3597c86505
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08623887B2

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