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Dichloromethane → 2-(4-Hydroxyphenyl)-5-pentylthiophene

HRID 2121297
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반응식

HRID 2121297 반응식
B(Br)(Br)Br.ClCCl.C[O:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[S:17][C:18]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])=[CH:19][CH:20]=2)=[CH:12][CH:11]=1>O>[OH:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[S:17][C:18]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])=[CH:19][CH:20]=2)=[CH:12][CH:11]=1
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참가 물질

5

반응물 3

HCID 6344Dichloromethane2회HCID 25134Boron tribromideHCID 234321132-(4-Methoxyphenyl)-5-pentylthiophene

생성물 1

HCID 234323142-(4-Hydroxyphenyl)-5-pentylthiophene수율 81.4%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of boron tribromide (3.2 cm3) and dichloromethane (30 cm3) was added dropwise to a solution of 2-(4-methoxyphenyl)-5-pentylthiophene (10.0 g) and dichloromethane (70 cm3) at 0° C. under an atmosphere of nitrogen. The reaction solution was stirred overnight at room temperature and water (100 cm3) added. The organic layer was separated off and the aqueous layer extracted with dichloromethane (2×100 cm3). The combined organic layers were washed with brine (2×100 cm3) and then dried (MgSO4), filtered and evaporated down. The residue was purified by column chromatography on silica gel using a 4:1 hexane/dichloromethane mixture as eluent and recrystallisation from hexane to yield 7.7 g of g 2-(4-hydroxyphenyl)-5-pentylthiophene, K 100-102° C., I.

후처리

  1. customThe organic layer was separated off
  2. extractionthe aqueous layer extracted with dichloromethane (2×100 cm3)
  3. washThe combined organic layers were washed with brine (2×100 cm3)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated down
  7. customThe residue was purified by column chromatography on silica gel using a 4:1 hexane/dichloromethane mixture as eluent
  8. customrecrystallisation from hexane

출처 및 근거

ORD 기록
ord-16905664bdd644e98b28daabbe53758f
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06696110B1

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