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

Hydrochloric Acid → 1,2-Bis(methylsulfonyl)-1,2-dimethylhydrazine

HRID 249369
노트
인쇄 미리보기

반응식

HRID 249369 반응식
Cl.Cl.[CH3:3][NH:4][NH:5][CH3:6].[CH3:7][S:8](Cl)(=[O:10])=[O:9].Cl>>[CH3:7][S:8]([N:4]([CH3:3])[N:5]([S:8]([CH3:7])(=[O:10])=[O:9])[CH3:6])(=[O:10])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 93801,2-Dimethylhydrazine dihydrochlorideHCID 31297Methanesulfonyl chloride

생성물 1

HCID 150448651,2-Bis(methylsulfonyl)-1,2-dimethylhydrazine수율 32.4%

실험 절차

1,2-Dimethylhydrazine dihydrochloride (2.6 g, 0.02 mol) was suspended in ice-cold dry pyridine (6 ml) and the mixture was stirred for 10 minutes. Methanesulfonyl chloride (5.0 g, 0.043 mol) was added in portions to this mixture, while maintaining the temperature between 0° and 10° C. After an additional 1 hour of stirring at 0° to 5° C., the reaction mixture was left in a freezer (-10° C.) overnight. The pH of the reaction mixture was adjusted to pH 1 with cold dilute hydrochloric acid. The solid that separated was filtered and recrystallized from ethanol (Norit A) to give 1.4 g (32%) of the title compound: m.p. 168°-169° C.; anal. (C4H12N2O4S2) C,H,N; 1H NMR (CDCl3) δ 3.1 [2s, 12H, 2(CH3SO2NCH3)].

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturewhile maintaining the temperature between 0° and 10° C
  2. stirringAfter an additional 1 hour of stirring at 0° to 5° C.
  3. waitthe reaction mixture was left in a freezer (-10° C.) overnight
  4. customThe solid that separated
  5. filtrationwas filtered
  6. customrecrystallized from ethanol (Norit A)

출처 및 근거

ORD 기록
ord-73f8c8477bce4e8d9e13c39348f1a3ba
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05214068

반응 노트

불러오는 중…