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

Water → 4-Chloro-N-[(1H-imidazol-2-yl)methyl]aniline

HRID 1179437
노트
인쇄 미리보기

반응식

HRID 1179437 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]=O.[Cl:8][C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=1.[BH4-].[Na+].O>CO>[Cl:8][C:9]1[CH:15]=[CH:14][C:12]([NH:13][CH2:6][C:2]2[NH:3][CH:4]=[CH:5][N:1]=2)=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 78124-ChloroanilineHCID 249551H-imidazole-2-carbaldehydeHCID 4311764Sodium borohydride

생성물 1

HCID 108460134-Chloro-N-[(1H-imidazol-2-yl)methyl]aniline수율 53.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

The solution of 2-imidazolecarboxaldehyde (570 mg, 5.9 mmol) and 4-chloroaniline (756 mg, 5.9 mmol) in methanol (5 ml) was stirred at 60° C. for 4 hours, and allowed to cool to room temperature. To the reaction was added NaBH4 (337 mg, 8.9 mmol), and the mixture was additionally stirred for an hour. Water (20 mL) was added to the reaction, which was extracted with ethyl acetate (50 mL). Organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (5% methanol in chloroform) to give the title compound (660 mg, 53%).

후처리

  1. extractionwas extracted with ethyl acetate (50 mL)
  2. dry with materialOrganic layer was dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (5% methanol in chloroform)

출처 및 근거

ORD 기록
ord-813eb3b18b5d45a98cf056db46d03476
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07279497B2

반응 노트

불러오는 중…