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Carbon Dioxide → Lithium 4-(morpholinomethyl)thiazole-2-carboxylate

HRID 546431
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인쇄 미리보기

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HRID 546431 반응식
[O:1]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]2[N:9]=[CH:10][S:11][CH:12]=2)[CH2:3][CH2:2]1.[C:13](=[O:15])=[O:14].C([Li:20])CCC>C(OCC)C>[O:1]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]2[N:9]=[C:10]([C:13]([O-:15])=[O:14])[S:11][CH:12]=2)[CH2:3][CH2:2]1.[Li+:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 280Carbon DioxideHCID 178425104-(Morpholinomethyl)thiazoleHCID 178418339Butyllithium

생성물 1

HCID 23712808Lithium 4-(morpholinomethyl)thiazole-2-carboxylate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
-78 °C

실험 절차

4-(Morpholinomethyl)thiazole (640 mg) was dissolved in diethyl ether (5 ml) in an argon atmosphere, and n-butyllithium (1.54N hexane solution, 2.50 ml) was added dropwise at −78° C. The reaction mixture was stirred for 10 minutes under ice cooling, and cooled again to −78° C. After blowing carbon dioxide into the reaction mixture for 20 minutes, it was heated to room temperature. The reaction mixture was concentrated under reduced pressure to obtain the title compound (873 mg) as crude yellow powder.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionwas added dropwise at −78° C
  2. customfor 20 minutes
  3. temperatureit was heated to room temperature
  4. concentrationThe reaction mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-64b8271cb2164c2a9604aa0661facf5e
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07935824B2

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