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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium borohydride → HCID 178521552, 화합물

HRID 657677
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HRID 657677 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]2[CH2:17][CH2:16][C:15](=[O:18])[CH2:14][CH2:13]2)=[CH:8][CH:7]=1.[BH4-].[Na+]>CO>[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C@H:12]2[CH2:17][CH2:16][C@H:15]([OH:18])[CH2:14][CH2:13]2)=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 23150298HCID 23150298, 화합물

생성물 1

HCID 178521552HCID 178521552, 화합물수율 68.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 4-[4-(3-chloropropoxy)phenyl]cyclohexanone (800 mg) in methanol (10 mL) is cooled to a temperature close to 0° C. Sodium borohydride (57 mg) is added and the mixture stirred for one hour at room temperature, then concentrated under reduced pressure. Water (15 mL) is added and the insoluble separated by filtration, rinsed with diethyl ether and dried under reduced pressure to give 550 mg of trans-4-[4-(3-chloropropoxy)phenyl]cyclohexanol as a white solid used without further purification.

후처리

  1. customclose to 0° C
  2. concentrationconcentrated under reduced pressure
  3. additionWater (15 mL) is added
  4. customthe insoluble separated by filtration
  5. washrinsed with diethyl ether
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-48ab2c9832bf4c94b8283dca0a36880c
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08076329B2

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