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

Hydrazine hydrate (1:1) → 5-ethyl-3-(trifluoromethyl)-1H-pyrazole

HRID 2043753
노트
인쇄 미리보기

반응식

HRID 2043753 반응식
[F:1][C:2]([F:11])([F:10])[C:3](=O)[CH2:4][C:5](=O)[CH2:6][CH3:7].O.[NH2:13][NH2:14]>C(O)(=O)C.O>[CH2:6]([C:5]1[NH:14][N:13]=[C:3]([C:2]([F:11])([F:10])[F:1])[CH:4]=1)[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 678642,4-Hexanedione, 1,1,1-trifluoro-

생성물 1

HCID 230062095-ethyl-3-(trifluoromethyl)-1H-pyrazole수율 59.2%

시약·촉매·용매 2

HCID 176Acetic Acid촉매HCID 962Water용매

실험 절차

A solution of 1,1,1-trifluoro-2,4-hexane-dione (2.4 g, 14.3 mmol), hydrazine hydrate (1.0 g, 19.0 mmol) and acetic acid (1 drop) in water (10 mL) was heated to reflux for 1 h. The reaction mixture was then cooled in an ice bath to form a white precipitate. The precipitate was then filtered, dissolved in chloroform and dried over MgSO4. The resulting solution was concentrated under reduced pressure to provide 1.39 g of the title compound. This compound was of sufficient purity to use in subsequent reactions.

후처리

  1. temperatureto reflux for 1 h
  2. temperatureThe reaction mixture was then cooled in an ice bath
  3. customto form a white precipitate
  4. filtrationThe precipitate was then filtered
  5. dissolutiondissolved in chloroform
  6. dry with materialdried over MgSO4
  7. concentrationThe resulting solution was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ea48f14783d245c187070bf9cebb8a9a
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586611B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트