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Sodium borohydride → 4-(p-Fluorophenyl)-3-cyclohexen-1-ol

HRID 1657559
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HRID 1657559 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][CH:9]=2)=[CH:4][CH:3]=1.[BH4-].[Na+]>C(O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH:9]=2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 226102684-(4-Fluorophenyl)cyclohex-3-en-1-one

생성물 1

HCID 215344654-(p-Fluorophenyl)-3-cyclohexen-1-ol수율 96%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 0.065 mole of 4-(p-fluorophenyl)-3-cyclohexen-1-one (obtained as in Example 7) and 6 g. of sodium borohydride in 130 ml. of ethanol is stirred at room temperature for about 5 hours. The bulk of the solvent is removed on a rotary evaporator and the residue diluted with water. The precipitated solid is collected on a filter and recrystallized from Skellysolve B to give a 96% yield of 4-(p-fluorophenyl)-3-cyclohexen-1-ol having a melting point of 73° to 74.5° C.

후처리

  1. customThe bulk of the solvent is removed on a rotary evaporator
  2. additionthe residue diluted with water
  3. customThe precipitated solid is collected on
  4. filtrationa filter
  5. customrecrystallized from Skellysolve B

출처 및 근거

ORD 기록
ord-9c2bafb466cb476e89c4de00865d83b5
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03960961

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