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

Diisopropyl Ether → HCID 178526613, 화합물

HRID 45853
노트
인쇄 미리보기

반응식

HRID 45853 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:14]=[CH:13][NH:12][N:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[I:15]N1C(=O)CCC1=O.C(OC(C)C)(C)C>CN(C)C=O>[I:15][C:14]1[C:10]([C:6]2[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)=[N:11][NH:12][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7914Diisopropyl EtherHCID 120273N-IodosuccinimideHCID 178526599HCID 178526599, 화합물

생성물 1

HCID 178526613HCID 178526613, 화합물수율 75%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
70 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

2.1 g (11 mmol) of 3-(3-nitrophenyl)-1H-pyrazole were dissolved in 25 ml of dry dimethylformamide and 2.63 g (11.7 mmol) of N-iodosuccinimide were added. After 5 hours under stirring at 70° C. the most part of solvent was removed in vacuo and an aqueous solution of sodium thiosulphate was added and the product extracted several times with dichloromethane. The organic phase was then dried over sodium sulphate and evaporated to give, after trituration with diisopropylether, 2.6 g (74%) of the title compound.

후처리

  1. customwas removed in vacuo
  2. additionan aqueous solution of sodium thiosulphate was added
  3. extractionthe product extracted several times with dichloromethane
  4. dry with materialThe organic phase was then dried over sodium sulphate
  5. customevaporated
  6. customto give

출처 및 근거

ORD 기록
ord-3864ce29c79c432bbfe7b99c63a31718
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541575B2

반응 노트

불러오는 중…