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

HCID 20388954, 화합물 → 3-(2-Methyl-1,3-thiazol-5-yl)propan-1-ol

HRID 616379
노트
인쇄 미리보기

반응식

HRID 616379 반응식
[CH3:1][C:2]1[S:3][C:4]([CH2:7][CH2:8][C:9](OC)=[O:10])=[CH:5][N:6]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH3:1][C:2]1[S:3][C:4]([CH2:7][CH2:8][CH2:9][OH:10])=[CH:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 20388954HCID 20388954, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 203889553-(2-Methyl-1,3-thiazol-5-yl)propan-1-ol수율 69.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

실험 절차

10.9 g of methyl 2-methyl-5-thiazole-propanoate in 70 ml of tetrahydrofuran was slowly added with stirring at 10°-15° C to a mixture of 125 ml of tetrahydrofuran and 3.42 g of lithium aluminum hydride at 10° C and the mixture was stirred for about 30 minutes. Then, tetrahydrofuran containing 20% water was slowly added and the mixture was filtered. The filter was washed with ethyl acetate and the filtrate was dried over magnesium sulfate and concentrated under reduced pressure to obtain 8.4 g of raw product which was rectified under reduced pressure to obtain 6.4g of 2-methyl-5-thiazole propanol with a boiling point of 106° C under 0.05 mm Hg.

후처리

  1. filtrationthe mixture was filtered
  2. washThe filter was washed with ethyl acetate
  3. dry with materialthe filtrate was dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customto obtain 8.4 g of raw product which

출처 및 근거

ORD 기록
ord-f329d76be58645709fdad2cefed6c71b
출처 데이터셋
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04073919

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트