2-(2-(Benzyloxy)-5-(tert-butyl)phenyl)-2-methylpropanenitrile → 2-(5-(tert-Butyl)-2-hydroxyphenyl)-2-methylpropanenitrile

HRID 2205444노트

반응식

HRID 2205444 반응식
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])=[CH:11][C:10]=1[C:19]([CH3:23])([CH3:22])[C:20]#[N:21])C1C=CC=CC=1>CO>[C:15]([C:12]1[CH:13]=[CH:14][C:9]([OH:8])=[C:10]([C:19]([CH3:23])([CH3:22])[C:20]#[N:21])[CH:11]=1)([CH3:18])([CH3:16])[CH3:17]

참가 물질

3

반응물 1

HCID 595441512-(2-(Benzyloxy)-5-(tert-butyl)phenyl)-2-methylpropanenitrile

생성물 1

HCID 595441652-(5-(tert-Butyl)-2-hydroxyphenyl)-2-methylpropanenitrile

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Pd (OH)2/C (2.0 g) and compound 7 (20.0 g, 0.104 mol) were stirred in MeOH (150 mL) at room temperature under hydrogen at 10 psi pressure for 16-18 hours. The mixture was then filtered through a pad of Celite®, and the filtrate was concentrated to give compound 15, which was used in the next reaction without further purification. 1H NMR (DMSO-d6; 400 MHz) δ 9.83 (s), δ 7.24 (s), δ 7.18 (m), δ 6.80 (m), δ 1.71 (s), δ 1.24 (s).

후처리

  1. filtrationThe mixture was then filtered through a pad of Celite®
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-fbe3f1b8be5e481d9eda56e5755227ae
출처 데이터셋
uspto-grants-2016_06
특허 번호
US09371287B2

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