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(1S,3R)-3-(dibenzylamino)-1-methylcyclohexanol → HCID 86676339, 화합물

HRID 2280732
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HRID 2280732 반응식
C([N:8](CC1C=CC=CC=1)[C@@H:9]1[CH2:14][CH2:13][CH2:12][C@:11]([CH3:16])([OH:15])[CH2:10]1)C1C=CC=CC=1.[H][H]>C(O)C.[OH-].[OH-].[Pd+2]>[NH2:8][C@@H:9]1[CH2:14][CH2:13][CH2:12][C@@:11]([CH3:16])([OH:15])[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 71237246(1S,3R)-3-(dibenzylamino)-1-methylcyclohexanolHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86676339HCID 86676339, 화합물수율 62.3%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매

실험 절차

A solution of (1S,3R)-3-(dibenzylamino)-1-methylcyclohexanol (5.0 g, 16.16 mmol) in ethanol (150 mL) was treated with palladium hydroxide on carbon and stirred under a balloon filled with hydrogen gas overnight. Upon completion of the reaction as indicated by LCMS the reaction mixture was filtered through a pad of celite and the filtrate concentrated to yield (1R,3R)-3-amino-1-methylcyclohexanol (1.3 g, 62%) as a thick yellow oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.87 (br. s., 1H), 1.64-1.74 (m, 1H), 1.47-1.59 (m, 2H), 1.21-1.40 (m, 4H), 1.11-1.20 (m, 1H), 1.02 (s, 3H); MS (ESI) m/z 130.2 [M+1]+.

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후처리

  1. customUpon completion of the reaction
  2. filtrationwas filtered through a pad of celite
  3. concentrationthe filtrate concentrated

출처 및 근거

ORD 기록
ord-8f28cd05ed034920ac2dc807d156b190
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09139534B2

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