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Water → [1-(4-Ethoxyphenyl)-2,2-difluorocyclopropyl]methanol

HRID 867911
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HRID 867911 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10]([C:12]1([C:17]2[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH3:25])=[CH:19][CH:18]=2)[CH2:14][C:13]1([F:16])[F:15])=O)C.O.[OH-].[Na+]>CCOCC>[CH2:24]([O:23][C:20]1[CH:19]=[CH:18][C:17]([C:12]2([CH2:10][OH:9])[CH2:14][C:13]2([F:15])[F:16])=[CH:22][CH:21]=1)[CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 6454760Cyclopropanecarboxylic acid, 1-(4-ethoxyphenyl)-2,2-difluoro-, ethyl ester, (+-)-HCID 21226445Aluminium lithium hydride

생성물 1

HCID 14346307[1-(4-Ethoxyphenyl)-2,2-difluorocyclopropyl]methanol수율 92%

시약·촉매·용매 1

HCID 3283
Diethyl Ether
용매
2회

실험 절차

To 1.0 g of lithium aluminium hydride in 120 ml of dry ether, at room temperature is added dropwise 5.4 g (0.02 moles) of ethyl-1-(4-ethoxyphenyl)-2,2-difluorocyclopropane-1-carboxylate in 20 ml of ether. The reaction mixture is stirred for 1 hr after which 1.0 ml of water 1.0 ml of 15% NaOH, followed by 3.0 ml of water are added. The solid precipitate is filtered off, washed with ether and the combined filtrates dried and concentrated under reduced pressure to yield (4.2 g) a colourless oil; nD 1.5129.

후처리

  1. additionare added
  2. filtrationThe solid precipitate is filtered off
  3. washwashed with ether
  4. customthe combined filtrates dried
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-fde7254ec6dd453eb4fb3ce98e9b32ea
출처 데이터셋
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04777185

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