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

p-Toluenesulfonic acid → Ethyl 3-(2,4-difluorophenyl)-3-oxopropanoate

HRID 2209979
노트
인쇄 미리보기

반응식

HRID 2209979 반응식
[F:1][C:2]1[CH:20]=[C:19]([F:21])[CH:18]=[CH:17][C:3]=1[C:4]([CH:6](C(OCC)=O)[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5].C1(C)C=CC(S(O)(=O)=O)=CC=1>O>[F:1][C:2]1[CH:20]=[C:19]([F:21])[CH:18]=[CH:17][C:3]=1[C:4]([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 15105381Diethyl (2,4-difluorobenzoyl)malonate

생성물 1

HCID 2758338Ethyl 3-(2,4-difluorophenyl)-3-oxopropanoate

시약·촉매·용매 1

HCID 962Water용매

실험 절차

41.4 g of the crude diethyl (2,4-difluorobenzoyl)malonate in 130 ml of water and 170 mg of p-toluenesulphonic acid are refluxed for 8.5 hours. The mixture is extracted using methylene chloride, and the methylene chloride phase is washed with water, dried over sodium sulphate and concentrated in vacuo.

후처리

  1. extractionThe mixture is extracted
  2. washthe methylene chloride phase is washed with water
  3. dry with materialdried over sodium sulphate
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-004f342da97a46c88ff818f4982d3639
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05457104

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트