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Potassium Cyanide → 2-(1-Bromonaphthalen-2-yl)acetonitrile

HRID 1855972
노트
인쇄 미리보기

반응식

HRID 1855972 반응식
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[CH2:12]Br.[C-:14]#[N:15].[K+]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C(Cl)Cl.O>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[CH2:12][C:14]#[N:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 9032Potassium CyanideHCID 378281-Bromo-2-(bromomethyl)naphthalene

생성물 1

HCID 2343772-(1-Bromonaphthalen-2-yl)acetonitrile

시약·촉매·용매 3

HCID 66133Benzyl triethylammonium chloride촉매HCID 962Water용매2회HCID 6344Dichloromethane용매2회

실험 절차

A mixture of 99 parts of 1-bromo-2-(bromomethyl)naphthalene, 103 parts of potassium cyanide and 1 part of benzyl triethylammonium chloride in 150 parts by volume of methylene chloride and 30 parts by volume of water is stirred at room temperature for about 72 hours. The mixture is then diluted with additional quantities of methylene chloride and water, the organic layer separated, dried over calcium sulfate, and concentrated to give α-(1-bromo-2-naphthyl)acetonitrile, as a solid.

후처리

  1. customthe organic layer separated
  2. dry with materialdried over calcium sulfate
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3bf92dfc906f4dae8a086f25c09d43de
출처 데이터셋
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04217306

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