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Methanol → 3-Phenoxybenzaldehyde bisulfite

HRID 1659653
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HRID 1659653 반응식
[O:1]([C:8]1[CH:9]=[C:10]([CH:14]2OCC[O:15]2)[CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CO.[S:21]([O-:24])([OH:23])=[O:22].[Na+]>O>[S:21](=[O:22])([OH:24])[OH:23].[O:1]([C:8]1[CH:9]=[C:10]([CH:11]=[CH:12][CH:13]=1)[CH:14]=[O:15])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 136438312-(3-Phenoxyphenyl)-1,3-dioxolaneHCID 23665763Sodium Bisulfite

생성물 1

HCID 205556583-Phenoxybenzaldehyde bisulfite수율 89.5%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of 24.2 g. of 2-(3-phenoxyphenyl)-1,3-dioxolane in 120 ml. of methanol a solution of 41.6 g. of sodium hydrogensulfite in 120 ml. of water is added, and the reaction mixture is boiled until no traces of starting compound can be detected by thin layer chromatography. The reaction mixture is cooled, the precipitated crystals are filtered off, washed with a 50% aqueous methanol solution and dried at 60° to 80° C. 27 g. (89.5%) of 3-phenoxybenzaldehyde bisulfite are obtained.

후처리

  1. temperatureThe reaction mixture is cooled
  2. filtrationthe precipitated crystals are filtered off
  3. washwashed with a 50% aqueous methanol solution
  4. customdried at 60° to 80° C

출처 및 근거

ORD 기록
ord-d6002f654b0342d4ba44673f09cdd13d
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04304938

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