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

Hydrazine → 3-(trifluoromethyl)-1H-pyrazol-5-amine

HRID 536333
노트
인쇄 미리보기

반응식

HRID 536333 반응식
[NH2:1]/[C:2](/OCC)=[CH:3]\[C:4](=O)[C:5]([F:8])([F:7])[F:6].[NH2:13][NH2:14]>CCO>[F:6][C:5]([F:8])([F:7])[C:4]1[NH:14][N:13]=[C:2]([NH2:1])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9321HydrazineHCID 151117544-Amino-4-ethoxy-1,1,1-trifluorobut-3-en-2-one

생성물 1

HCID 196233053-(trifluoromethyl)-1H-pyrazol-5-amine

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
80 °C

실험 절차

A mixture of (E)-4-amino-4-ethoxy-1,1,1-trifluorobut-3-en-2-one (5.00 g, 27 mmol) and hydrazine (1.05 g) in anhydrous EtOH (20 mL) was stirred at 80° C. in a sealed vial overnight. The reaction was quenched with water (50 mL), and extracted with EtOAc (100 ml, then 2×50 mL). The EtOAc layers were combined and sequentially washed with water (25 mL), brine (25 mL), dried over Na2SO4 and evaporated to give a light brown oily residue. The crude product was purified by silica chromatography (30-100% EtOAc in hexanes gradient) to give 5-(trifluoromethyl)-1H-pyrazol-3-amine as an off white solid; ESMS m/z 152.0 (M+H+).

후처리

  1. customThe reaction was quenched with water (50 mL)
  2. extractionextracted with EtOAc (100 ml
  3. washsequentially washed with water (25 mL), brine (25 mL)
  4. dry with materialdried over Na2SO4
  5. customevaporated
  6. customto give a light brown oily residue
  7. customThe crude product was purified by silica chromatography (30-100% EtOAc in hexanes gradient)

출처 및 근거

ORD 기록
ord-3a987e84a18b4d508bbce2aee4d78131
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859574B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트