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

Sulfuryl chloride → 5-Bromo-2-chloro-1,3-benzothiazole

HRID 1965861
노트
인쇄 미리보기

반응식

HRID 1965861 반응식
S(Cl)([Cl:4])(=O)=O.[Br:6][C:7]1[CH:8]=[CH:9][C:10]2[S:14][C:13](S)=[N:12][C:11]=2[CH:16]=1>>[Br:6][C:7]1[CH:8]=[CH:9][C:10]2[S:14][C:13]([Cl:4])=[N:12][C:11]=2[CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24648Sulfuryl chlorideHCID 178527757HCID 178527757, 화합물

생성물 1

HCID 202512695-Bromo-2-chloro-1,3-benzothiazole수율 100%

실험 절차

To sulfuryl dichloride (5 mL) was added 5-bromobenzo[d]thiazole-2-thiol (450 mg, 1.8 mmol) portionwise. The mixture was stirred at rt for 1 hour and heated at 50° C. for 15 min. After cooling to rt, the reaction mixture was slowly poured onto ice (50 g) and the resulting suspension was stirred for 30 min. Solid was collected through filtration and washed with water (10 mL) and dried under high vacuum to afford 5-bromo-2-chlorobenzo[d]thiazole as a pink solid (470 mg, 100%). MS (ESI) m/z 248 (M+H+).

후처리

  1. temperatureheated at 50° C. for 15 min
  2. temperatureAfter cooling to rt
  3. additionthe reaction mixture was slowly poured onto ice (50 g)
  4. stirringthe resulting suspension was stirred for 30 min
  5. filtrationSolid was collected through filtration
  6. washwashed with water (10 mL)
  7. customdried under high vacuum

출처 및 근거

ORD 기록
ord-28443ae781844559a83c7081fbfc3abf
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08420052B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트