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Sodium Cyanide → 2-(3-(2,6-Dimethylbenzyloxy)-2-methoxyphenyl)acetonitrile

HRID 1958863
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HRID 1958863 반응식
CS(O[CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][C:15]2[C:20]([CH3:21])=[CH:19][CH:18]=[CH:17][C:16]=2[CH3:22])[C:8]=1[O:23][CH3:24])(=O)=O.[C-:25]#[N:26].[Na+]>CN(C=O)C.CCOC(C)=O>[CH3:22][C:16]1[CH:17]=[CH:18][CH:19]=[C:20]([CH3:21])[C:15]=1[CH2:14][O:13][C:9]1[C:8]([O:23][CH3:24])=[C:7]([CH2:6][C:25]#[N:26])[CH:12]=[CH:11][CH:10]=1
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참가 물질

5

반응물 2

HCID 8929Sodium CyanideHCID 866570093-(2,6-Dimethylbenzyloxy)-2-methoxybenzyl methanesulfonate

생성물 1

HCID 669593842-(3-(2,6-Dimethylbenzyloxy)-2-methoxyphenyl)acetonitrile

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

실험 절차

The solution of 3-(2,6-dimethylbenzyloxy)-2-methoxybenzyl methanesulfonate (Step C, 8.8 g, 30.26 mmol) and NaCN (1.60 g, 32.6 mmol) in dry DMF (40 ml) was heated at 85° C. for 18 hours then cooled and diluted with EtOAc (50 ml). The organic layer was washed with water (30 ml), concentrated, and passed through short silica gel column using methylene chloride to give the title compound as a yellow solid.

후처리

  1. temperaturethen cooled
  2. washThe organic layer was washed with water (30 ml)
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a69f18c5f88548519e873ae801e9f88d
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08410154B2

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