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Toluene → Ethyl 4-(3-bromopropyl)benzoate

HRID 2083111
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HRID 2083111 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 one 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. Boiling point0.1 : 105° - 107° C.

후처리

  1. customThe solvent and the thionyl chloride in excess were removed under reduced pressure
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • additionafter addition of 400 ml of absolute ethanol to the residue the mixture
  • temperaturewas heated for one hour to the boiling point
  • customIt was evaporated under reduced pressure
  • washwashed neutral with a saturated NaHCO3 -solution
  • distillationThe organic phase was distilled off
  • dry with materialafter drying with MgSO4
  • custom105° - 107° C.
  • 출처 및 근거

    ORD 기록
    ord-bb5681c071f64926bc95c366d4df30ad
    출처 데이터셋
    uspto-grants-1978_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04083990

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