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1-Benzyl-3-ethyl-4-hydroxypiperidine → 3-Ethylpiperidin-4-ol

HRID 396305
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HRID 396305 반응식
C([N:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH:10]([CH2:15][CH3:16])[CH2:9]1)C1C=CC=CC=1>CO.[H][H].[OH-].[Pd+2].[OH-]>[CH2:15]([CH:10]1[CH:11]([OH:14])[CH2:12][CH2:13][NH:8][CH2:9]1)[CH3:16]
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참가 물질

5

반응물 1

HCID 230037101-Benzyl-3-ethyl-4-hydroxypiperidine

생성물 1

HCID 219737483-Ethylpiperidin-4-ol

시약·촉매·용매 3

HCID 9942167Palladium hydroxide촉매2회HCID 887Methanol용매2회HCID 178418361HCID 178418361, 화합물용매

실험 절차

A mixture of 1-benzyl-3-ethyl-4-hydroxypiperidine (5.0 g, 22.0 mmole) and palladium hydroxide (1.5 g) in methanol (100 ml) was stirred at 5.0 g, 22.0 mmole) and palladium hydroxide (1.5 g) in methanol (100 ml) was stirred at 50-55° C. in hydrogen atmosphere (1 atm.) for 20 hr. The catalyst was filtered off, washed with methanol, and filtrate was concentrated to dryness to give 3-ethyl-4-hydroxypiperidine as oil. Yield 2.9 g (94%), C7H15NO, m/z 130 (M+1).

후처리

  1. filtrationThe catalyst was filtered off
  2. washwashed with methanol, and filtrate
  3. concentrationwas concentrated to dryness

출처 및 근거

ORD 기록
ord-8eda4e99072d423ca3f7f36185454433
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06608078B2

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