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

Ethanol → 4-Bromo-3-fluorobenzaldehyde

HRID 346263
노트
인쇄 미리보기

반응식

HRID 346263 반응식
C([O:4][CH:5](OC(=O)C)[C:6]1[CH:11]=[CH:10][C:9]([Br:12])=[C:8]([F:13])[CH:7]=1)(=O)C.C(O)C.O.S(=O)(=O)(O)O>CCOCC>[Br:12][C:9]1[CH:10]=[CH:11][C:6]([CH:5]=[O:4])=[CH:7][C:8]=1[F:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 962WaterHCID 1118Sulfuric AcidHCID 536330654-Bromo-3-fluorobenzylidene diacetate

생성물 1

HCID 27834114-Bromo-3-fluorobenzaldehyde

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A mixture of 4-bromo-3-fluorobenzylidene diacetate (15 g), ethanol (41 ml), water (41 ml) and concentrated sulphuric acid (4 ml) was heated to reflux for 3 hours. After cooling, ether (300 ml) was added and the aqueous layer separated. The organic phase was washed with saturated sodium carbonate and brine before drying over anhydrous magnesium sulphate and evaporation in vacuo. 4-Bromo-3-fluorobenzaldehyde was obtained as a solid (7.3 g).

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 3 hours
  3. temperatureAfter cooling
  4. customthe aqueous layer separated
  5. washThe organic phase was washed with saturated sodium carbonate and brine
  6. dry with materialbefore drying over anhydrous magnesium sulphate and evaporation in vacuo

출처 및 근거

ORD 기록
ord-b2bf3b052c1e4a8cba5a34f25d501af9
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05061726

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트