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

Dichloroacetaldehyde → 2,2-Dichloroacetaldehyde tosylhydrazone

HRID 352061
노트
인쇄 미리보기

반응식

HRID 352061 반응식
[S:1]([NH:11][NH2:12])([C:4]1[CH:10]=[CH:9][C:7]([CH3:8])=[CH:6][CH:5]=1)(=[O:3])=[O:2].[Cl:13][CH:14]([Cl:17])[CH:15]=O>C(O)(=O)CC>[S:1]([NH:11][N:12]=[CH:15][CH:14]([Cl:17])[Cl:13])([C:4]1[CH:5]=[CH:6][C:7]([CH3:8])=[CH:9][CH:10]=1)(=[O:2])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6576DichloroacetaldehydeHCID 15303P-Toluenesulfonylhydrazide

생성물 1

HCID 671758942,2-Dichloroacetaldehyde tosylhydrazone수율 70%

시약·촉매·용매 1

HCID 1032Propionic Acid용매

실험 절차

Tosylhydrazine (234 g, 1.26 mol) was suspended in propionic acid (2 L) and dichloroacetaldehyde (142 g, 1.26 mol) was added at 15-20° C. The mixture was stirred at room temperature for 2 hours and under ice-cooling for 3 hours. The precipitated crystals were collected by filtration and washed with toluene. The crystals were dried under reduced pressure to give 2,2-dichloroacetaldehyde tosylhydrazone (247 g, yield 70%).

후처리

  1. temperaturecooling for 3 hours
  2. filtrationThe precipitated crystals were collected by filtration
  3. washwashed with toluene
  4. customThe crystals were dried under reduced pressure

출처 및 근거

ORD 기록
ord-15bbb390251345f0a7952e3d8da65690
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06743924B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트