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

Azobisisobutyronitrile → HCID 19385620, 화합물

HRID 2399456
노트
인쇄 미리보기

반응식

HRID 2399456 반응식
[CH3:1][C:2]1[CH:20]=[CH:19][C:5]([O:6][C:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)([CH3:12])[C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1.C1C(=O)N([Br:28])C(=O)C1.CC(N=NC(C#N)(C)C)(C#N)C>C(Cl)(Cl)(Cl)Cl>[Br:28][CH2:1][C:2]1[CH:20]=[CH:19][C:5]([O:6][C:7]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)([CH3:12])[C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 19385683HCID 19385683, 화합물

생성물 1

HCID 19385620HCID 19385620, 화합물수율 66.9%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of the product of Step B (26 mg, 0.096 mmol) NBS (16 mg, 0.95 eq) and AIBN (2 mg, catalytic amount) in CCl4 (2 mL) was heated to reflux for 1 hour and then concentrated in vacuo. The residue was purified on a silica gel flash chromatography column (125×20 mm) eluted with 5% ethyl acetate/hexane to yield 21 mg (62%) of the title compound.

후처리

  1. temperatureto reflux for 1 hour
  2. concentrationconcentrated in vacuo
  3. customThe residue was purified on a silica gel flash chromatography column (125×20 mm)
  4. washeluted with 5% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-ce4be18d8d0e4d068c94bc7b84389c25
출처 데이터셋
uspto-grants-1995_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05449682

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트