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

Lithium dimethylamide → 1,3-Dimethyl-2-dimethylaminoimidazolidinium nitrate

HRID 2116856
노트
인쇄 미리보기

반응식

HRID 2116856 반응식
[N+:1]([O-:4])([O-:3])=[O:2].[CH3:5][NH+:6]1[CH2:10][CH2:9][N:8]([CH3:11])[CH:7]1Cl.[CH3:13][N-:14][CH3:15].[Li+]>C(#N)C>[N+:1]([O-:4])([O-:3])=[O:2].[CH3:5][NH+:6]1[CH2:10][CH2:9][N:8]([CH3:11])[CH:7]1[N:14]([CH3:15])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5152226Lithium dimethylamideHCID 693110371,3-Dimethyl-2-chloroimidazolidinium nitrate

생성물 1

HCID 693123831,3-Dimethyl-2-dimethylaminoimidazolidinium nitrate수율 92.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3.00 g (15.34 mmol) of 1,3-dimethyl-2-chloroimidazolidinium nitrate and 0.78 g (15.29 mmol) of lithium dimethylamide are dissolved in 20 ml of acetonitrile under a protective-gas atmosphere (argon). The reaction mixture is stirred for 5 hours at room temperature, and LiCl is subsequently filtered off. The salt LiCl is washed with 5 ml of acetonitrile, and the organic phases are combined. The solvent is distilled off, and the residue is dried under reduced pressure at 7 Pa and 50° C., giving 2.91 g of 1,3-dimethyl-2-dimethylaminoimidazolidinium nitrate as a liquid, corresponding to a yield of 92.2%.

후처리

  1. filtrationLiCl is subsequently filtered off
  2. washThe salt LiCl is washed with 5 ml of acetonitrile
  3. distillationThe solvent is distilled off
  4. customthe residue is dried under reduced pressure at 7 Pa and 50° C.

출처 및 근거

ORD 기록
ord-5ffac93d34464dd4ac156e277a65eff1
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07439395B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트