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

Acetonitrile → 4-bromo-5-(4-chlorophenyl)-1-methyl-1H-imidazole

HRID 1506657
노트
인쇄 미리보기

반응식

HRID 1506657 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]([CH3:13])[CH:10]=CN=2)=[CH:4][CH:3]=1.C1C(=O)N([Br:21])C(=O)C1.[C:22](#[N:24])C>>[Br:21][C:22]1[N:24]=[CH:10][N:9]([CH3:13])[C:8]=1[C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6342AcetonitrileHCID 67184N-bromobutanimideHCID 10856331(4-Chlorophenyl)-1-methyl-1H-imidazole

생성물 1

HCID 251721464-bromo-5-(4-chlorophenyl)-1-methyl-1H-imidazole

반응 조건

온도
0 °C

실험 절차

(4-Chlorophenyl)-1-methyl-1H-imidazole (3 g, 15.5 mmol) was dissolved in ACN (150 mL) and cooled to 0° C. NBS (2.76 g, 15.5 mmol) was added in 3 portions over 5 min. The reaction was stirred at 0° C. for 20 min then let warm to ambient temperature. Solvents were removed in vacuo and the residue partitioned between EtOAc and 20% aqueous KH2PO4. The organics were separated, washed with saturated aqueous NaHCO3, and dried with saturated aqueous NaCl. Solvents were removed in vacuo and the residue purified by column chromatography on silica to provide the desired product. MS (m/z) 273.1 [M+H]+.

후처리

  1. temperaturethen let warm to ambient temperature
  2. customSolvents were removed in vacuo
  3. customthe residue partitioned between EtOAc and 20% aqueous KH2PO4
  4. customThe organics were separated
  5. washwashed with saturated aqueous NaHCO3
  6. dry with materialdried with saturated aqueous NaCl
  7. customSolvents were removed in vacuo
  8. customthe residue purified by column chromatography on silica

출처 및 근거

ORD 기록
ord-41c6eccd80504082ae7e6b03564163d4
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09220710B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트