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

Acetic Acid → 2-(2-Nitro-1-propen-1-yl)thiophene

HRID 1875342
노트
인쇄 미리보기

반응식

HRID 1875342 반응식
C([C:3]1[CH:7]=[CH:6][S:5][CH:4]=1)=O.[N+:8]([CH2:11][CH3:12])([O-:10])=[O:9].[CH2:13](N)CCC.C(O)(=O)C>>[N+:8]([C:11]([CH3:13])=[CH:12][C:6]1[S:5][CH:4]=[CH:3][CH:7]=1)([O-:10])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 176Acetic AcidHCID 6587NitroethaneHCID 8007ButylamineHCID 681353-Thiophenecarboxaldehyde

생성물 1

HCID 2382342-(2-Nitro-1-propen-1-yl)thiophene

반응 조건

온도
80 °C

실험 절차

5.0 g (44.6 mmol) 3-formylthiophene are dissolved together with 8.9 ml (124.8 mmol) nitroethane, 5.3 ml (53.5 mmol) butylamine in 25.1 ml glacial acetic acid (454.7 mmol) and heated to 80° C. After two hours the mixture is cooled and the precipitate formed is suction filtered and washed with copious amounts of water. The crude product thus obtained is dissolved in ethyl acetate, dried on sodium sulphate and evaporated down i. vac.

후처리

  1. temperatureAfter two hours the mixture is cooled
  2. customthe precipitate formed
  3. filtrationfiltered
  4. washwashed with copious amounts of water

출처 및 근거

ORD 기록
ord-15cbc30eed7840f59731c28708170544
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309542B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트