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Toluene → Ethyl 4-(3-bromopropyl)benzoate

HRID 839840
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반응식

HRID 839840 반응식
[Br:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1.S(Cl)(Cl)=O.[C:18]1(C)C=CC=C[CH:19]=1>>[CH2:18]([O:10][C:9](=[O:11])[C:8]1[CH:12]=[CH:13][C:5]([CH2:4][CH2:3][CH2:2][Br:1])=[CH:6][CH:7]=1)[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1140TolueneHCID 24386Thionyl ChlorideHCID 2377854-(3-Bromopropyl)benzoic acid

생성물 1

HCID 12748306Ethyl 4-(3-bromopropyl)benzoate

실험 절차

100 g 4-(3-Bromo-propyl)-benzoic acid (JACS 65, 2281 (1943)), 400 ml of toluene and 80 ml of thionyl chloride were refluxed for 4 hours. The solvent and the thionyl chloride in excess were removed under reduced pressure and after addition of 400 ml of absolute ethanol to the residue the mixture was heated for 1 hour to the boiling point. It was evaporated under reduced pressure, the residue was taken up in benzene and washed neutral with a saturated NaHCO3 -solution. The organic phase was distilled off after drying with MgSO4.

후처리

  1. customThe solvent and the thionyl chloride in excess were removed under reduced pressure
  2. additionafter addition of 400 ml of absolute ethanol to the residue the mixture
  3. temperaturewas heated for 1 hour to the boiling point
  4. customIt was evaporated under reduced pressure
  5. washwashed neutral with a saturated NaHCO3 -solution
  6. distillationThe organic phase was distilled off
  7. dry with materialafter drying with MgSO4

출처 및 근거

ORD 기록
ord-a9c03a3498be42c2a93d10fe5ce8e229
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04097496

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