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Ethanol → Ethyl 3-(4-methoxybenzoyl)propionate

HRID 1110019
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인쇄 미리보기

반응식

HRID 1110019 반응식
[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]([C:7]([CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[O:8])=[CH:5][CH:4]=1.S(=O)(=O)(O)O.[CH2:21](O)[CH3:22]>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:7]([CH2:9][CH2:10][C:11]([O:13][CH2:21][CH3:22])=[O:12])=[O:8])=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 766134-Methoxy-gamma-oxobenzenebutanoic acid

생성물 1

HCID 585132Ethyl 3-(4-methoxybenzoyl)propionate

실험 절차

21 g of 3-(4-methoxybenzoyl)propionic acid were heated under reflux for 51/4 hours in 350 ml of ethanol after addition of 7.3 ml of concentrated sulfuric acid The reaction mixture was worked up by concentrating it, taking up the remaining residue in 100 ml of water and extracting the mixture with dichloromethane. The organic phase was separated, washed with 50 ml of saturated aqueous sodium bicarbonate solution, then washed with water until neutral, dried and concentrated. 23.3 g of crude ethyl 3-(4-methoxybenzoyl)-propionate were obtained as a yellowish, crystallizing oil.

후처리

concentration
by concentrating it
  • extractionextracting the mixture with dichloromethane
  • customThe organic phase was separated
  • washwashed with 50 ml of saturated aqueous sodium bicarbonate solution
  • washwashed with water until neutral,
  • customdried
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-b53944b32fa44caa99cf3ba0cc6fea17
    출처 데이터셋
    uspto-grants-1994_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05324725

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