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

Imidazole → 1-[2-(2-methyl-1,3-dioxolan-2-yl)propyl]-1H-imidazole

HRID 1583425
노트
인쇄 미리보기

반응식

HRID 1583425 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[CH3:6][O-].[Na+].[CH3:9][C:10]1([CH2:15][CH2:16]CBr)[O:14][CH2:13][CH2:12][O:11]1>CN(C)C=O>[CH3:9][C:10]1([CH:15]([CH3:16])[CH2:6][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)[O:11][CH2:12][CH2:13][O:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 5600542-(3-Bromopropyl)-2-methyl-1,3-dioxolaneHCID 10942334Sodium Methoxide

생성물 1

HCID 202606171-[2-(2-methyl-1,3-dioxolan-2-yl)propyl]-1H-imidazole수율 47.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A suspension of 29.0 g of imidazole and 23.1 g of sodium methoxide in 385 ml of dimethylformamide was stirred for 30 minutes and cooled in an ice bath as 85.8 g of 3-(2-methyl-1,3-dioxolan-2-yl)propyl bromide was added dropwise. The resulting mixture was maintained at room temperature for 30 minutes and heated to reflux for 1 hour. The solvent was evaporated in vacuo, the residue diluted with acetone and filtered. The filtrate was concentrated and the residue was distilled to afford 37.9 g (47%) of 1-[2-(2-methyl-1,3-dioxolan-2-yl)propyl]-1H-imidazole as a colorless oil, bp 102°-108° C./0.1 mm.

후처리

  1. additionwas added dropwise
  2. temperatureheated
  3. temperatureto reflux for 1 hour
  4. customThe solvent was evaporated in vacuo
  5. additionthe residue diluted with acetone
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated
  8. distillationthe residue was distilled

출처 및 근거

ORD 기록
ord-a662a8656dc34ca2baa53b5404a660f5
출처 데이터셋
uspto-grants-1985_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04551460

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트