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

Ethanol → HCID 54280119, 화합물

HRID 1722750
노트
인쇄 미리보기

반응식

HRID 1722750 반응식
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[S:8])=[CH:5][CH:4]=1.C(O)C.Cl[CH:16]([CH3:20])[C:17](=O)[CH3:18]>CCOCC>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]2[S:8][C:16]([CH3:20])=[C:17]([CH3:18])[N:9]=2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 200263-Chloro-2-butanone2회HCID 7368274-Methoxybenzenecarbothioamide

생성물 1

HCID 54280119HCID 54280119, 화합물수율 87.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a stirred mixture of 65.1 g (4-methoxy)thiobenzamide and 156 ml ethanol was added dropwise 50.1 g 3-chloro-2-butanone, and the reaction mixture was heated at reflux for 3 hours. An additional 6.1 g 2-chloro-3-butanone was added and heating was continued for an additional hour. The reaction mixture was cooled, 300 ml ether added, and the solid which precipitated was collected and dried to give 74.5 g 2-(4-methoxyphenyl)-4,5-di-methylthiazole in the form of its hydrochloride monohydrate, m.p. 166-170° C.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 3 hours
  3. temperatureheating
  4. waitwas continued for an additional hour
  5. temperatureThe reaction mixture was cooled
  6. customthe solid which precipitated
  7. customwas collected
  8. customdried

출처 및 근거

ORD 기록
ord-a21e6ef65e0d4a5e80e8e52a13fadd73
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04857539

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트