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Sodium borohydride → 1-Benzyl-3-(trifluoromethyl)piperidin-4-ol

HRID 396300
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HRID 396300 반응식
[BH4-].[Na+].[CH2:3]([N:10]1[CH2:15][CH2:14][C:13](=[O:16])[CH:12]([C:17]([F:20])([F:19])[F:18])[CH2:11]1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>CO>[CH2:3]([N:10]1[CH2:15][CH2:14][CH:13]([OH:16])[CH:12]([C:17]([F:20])([F:18])[F:19])[CH2:11]1)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 230036951-Benzyl-3-(trifluoromethyl)piperidin-4-one

생성물 1

HCID 230037031-Benzyl-3-(trifluoromethyl)piperidin-4-ol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Sodium borohydride (0.6 g, 16.0 mmole) was added to the stirred solution of 1-benzyl-3-trifluoromethylpiperidin-4-one (2.1 g, 8.2 mmole) in methanol (25 ml) at 0-5° C. over a period of 5 min, and stirring was continued for 2 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water (20 ml) and extracted with chloroform. The chloroform extract was dried over sodium sulphate and concentrated to dryness to furnish 1-benzyl-4-hydroxy-3-trifluoromethylpiperidine as oil. Yield 1.8 g (85%), C13H16F3NO, m/z 259 (M+1).

후처리

  1. concentrationThe reaction mixture was concentrated to dryness
  2. customtriturated with water (20 ml)
  3. extractionextracted with chloroform
  4. extractionThe chloroform extract
  5. dry with materialwas dried over sodium sulphate
  6. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-23e1ecd6081d486199191f55ef644b61
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06608078B2

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