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Iodine → 3-(4-Hydroxyphenyl)-2,2-dimethylpropanoic acid ethyl ester

HRID 1417100
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HRID 1417100 반응식
Br[C:2]([CH3:9])([CH3:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].C([O:13][C:14]1[CH:21]=[CH:20][C:17]([CH:18]=O)=[CH:16][CH:15]=1)(=O)C.II>C1(C)C=CC=CC=1.[Zn].[Pd]>[CH2:6]([O:5][C:3](=[O:4])[C:2]([CH3:9])([CH3:8])[CH2:18][C:17]1[CH:16]=[CH:15][C:14]([OH:13])=[CH:21][CH:20]=1)[CH3:7]
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참가 물질

7

반응물 3

HCID 807IodineHCID 11745Propanoic acid, 2-bromo-2-methyl-, ethyl ester2회HCID 70144Benzaldehyde, 4-(acetyloxy)-

생성물 1

HCID 461805253-(4-Hydroxyphenyl)-2,2-dimethylpropanoic acid ethyl ester수율 14.6%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 23994
Zinc
촉매
HCID 1140Toluene용매2회

실험 절차

A slurry containing 24.6 g of zinc dust in 100 ml dry toluene was treated dropwise with a solution containing 73.5 g of ethyl bromoisobutyrate and 65 g of 4-acetoxybenzaldehyde in 200 ml dry toluene. A crystal of iodine was added to initiate the reaction and the mixture was heated to reflux overnight. An additional equivalent of ethyl bromoisobutyrate was added and reflux was continued for 24 hours. After cooling, the filtrate was hydrogenated over palladium and the residue purified by flash chromatography to give 12.2 g of 3-(4-hydroxyphenyl)-2,2-dimethylpropanoic acid ethyl ester as an oil.

후처리

  1. additionwas treated dropwise with a solution
  2. customthe reaction
  3. temperaturethe mixture was heated
  4. temperatureto reflux overnight
  5. temperaturereflux
  6. temperatureAfter cooling
  7. customthe residue purified by flash chromatography

출처 및 근거

ORD 기록
ord-7f5059bfc63a4f7c8c201eff0253daba
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05917057

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