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Water → Ethyl 2-formyl-3-(1-naphthyl)propionate

HRID 1248304
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반응식

HRID 1248304 반응식
[C:1]1([CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH:18](OCC)=[O:19].[H-].[Na+].O>COCCOC>[CH:18]([CH:12]([CH2:11][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1)[C:13]([O:15][CH2:16][CH3:17])=[O:14])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8025Ethyl formateHCID 24758Sodium hydrideHCID 10966256Ethyl 3-(1-naphthyl)propanoate

생성물 1

HCID 19592256Ethyl 2-formyl-3-(1-naphthyl)propionate수율 79.4%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A mixture of ethyl 3-(1-naphthyl)propionate (18.01 g) and ethyl formate (8.88 g) was added to a suspension of sodium hydride (57% dispersion in oil, 4.43 g) in 1,2-dimethoxyethane stirred at 5°, and the mixture was stirred at 5° for one hour and allowed to warm to room temperature. Water (300 ml) was added and the mixture was extracted with chloroform and the residual aqueous phase adjusted to pH 4 with hydrochloric acid: the mixture was extracted with ether and the extracts evaporated to give ethyl 2-formyl-3-(1-naphthyl)propionate (16.05 g) as an oil.

후처리

  1. stirringthe mixture was stirred at 5° for one hour
  2. extractionthe mixture was extracted with chloroform
  3. extractionthe mixture was extracted with ether
  4. customthe extracts evaporated

출처 및 근거

ORD 기록
ord-99247b5bdc684eec82a5a7e4f4234595
출처 데이터셋
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04523015

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