홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Chloroacetyl chloride → 2-chloro-N-(4-cyanophenyl)acetamide

HRID 535993
노트
인쇄 미리보기

반응식

HRID 535993 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.[Cl:17][CH2:18][C:19](Cl)=[O:20]>C(Cl)Cl>[Cl:17][CH2:18][C:19]([NH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1)=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6577Chloroacetyl chlorideHCID 8471TriethylamineHCID 133964-Aminobenzonitrile

생성물 1

HCID 21680152-chloro-N-(4-cyanophenyl)acetamide수율 92.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
26 °C

실험 절차

A mixture of 4-Amino benzonitrile (1.0 g, 0.0084 mol) and triethyl amine (1 ml, 0.010 mol) was taken in DCM (15 ml). Chloro acetyl chloride (0.67 ml, 0.0084 mol) was added slowly and stirred for 22 hours at 25-27° C. Solvent was removed and the residue was dissolved in ethyl acetate (20 ml), washed with water (1×15 ml) followed by brine (2×15 ml). The organic layer was dried over Na2SO4 and the solvent was removed to get pure 2-chloro-N-(4-cyano-phenyl)-acetamide (1.51 g, 92%).

후처리

  1. customSolvent was removed
  2. dissolutionthe residue was dissolved in ethyl acetate (20 ml)
  3. washwashed with water (1×15 ml)
  4. dry with materialThe organic layer was dried over Na2SO4
  5. customthe solvent was removed

출처 및 근거

ORD 기록
ord-57208d7d08974019b74f0f94ff07a99a
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859566B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트