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Boron tribromide → 4-[6-(2,3-Dihydroxyphenyl)hexyloxy]benzoic acid

HRID 1494237
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반응식

HRID 1494237 반응식
C[O:2][C:3](=[O:27])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([O:23]C)[C:18]=2[O:25]C)=[CH:6][CH:5]=1.B(Br)(Br)Br>C(Cl)Cl>[OH:25][C:18]1[C:19]([OH:23])=[CH:20][CH:21]=[CH:22][C:17]=1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][O:10][C:7]1[CH:6]=[CH:5][C:4]([C:3]([OH:27])=[O:2])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 149863444-[6-(2,3-Dimethoxyphenyl)hexyloxy]benzoic acid methyl ester

생성물 1

HCID 149863454-[6-(2,3-Dihydroxyphenyl)hexyloxy]benzoic acid수율 42%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To 0.80 g (2.2 mmol) of 4-[6-(2,3-dimethoxyphenyl)hexyloxy]benzoic acid methyl ester in 25 mL of methylene chloride stirred and cooled at -70° was added 8.0 mL of 1M boron tribromide in methylene chloride. The reaction mixture was stirred at -70° for 30 minutes and at -20° for 7 hours. Workup as in example 32 and recrystallization from ethyl acetate-hexane gave 0.30 g (42% yield), mp 170°-172° of 4-[6-(2,3-dihydroxyphenyl)hexyloxy]benzoic acid.

후처리

  1. temperaturecooled at -70°
  2. customWorkup as in example 32 and recrystallization from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-ac1359930020402ead1f9aa002ef3c1a
출처 데이터셋
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05025036

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