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Acetone → HCID 19917093, 화합물

HRID 1464764
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HRID 1464764 반응식
[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=2)[CH:9]=[O:10])=[CH:2]1.C(=O)([O-])[O-].[K+].[K+].[CH3:20][C:21]([CH3:23])=[O:22]>>[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:7]=[C:8]([CH:9]([OH:10])[CH2:20][C:21](=[O:22])[CH3:23])[CH:11]=[CH:12][CH:13]=2)=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 180AcetoneHCID 11430Potassium CarbonateHCID 45475263-(Thiophen-3-yl)benzaldehyde

생성물 1

HCID 19917093HCID 19917093, 화합물

실험 절차

300 mg of 3-(3-thienyl)benzaldehyde was dissolved in 3 ml of acetone, and 441 mg of potassium carbonate was added. The mixture was stirred overnight at s room temperature, and then the solvent was evaporated. The residue was worked up in a customary manner, and purified by medium-pressure liquid chromatography [hexane/ethyl acetate =3/1]to give 1-[3-(3-thienyl)phenyl]-3-oxo-1-butanol as a colorless oil.

후처리

  1. customthe solvent was evaporated
  2. custompurified by medium-pressure liquid chromatography [hexane/ethyl acetate =3/1]to

출처 및 근거

ORD 기록
ord-2a74735c8a6d431a81c4b82bd78d6418
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05306728

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