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

Methanol → 2-Isopropyl-4-(4-fluorophenyl)-3-butenoic acid

HRID 1395609
노트
인쇄 미리보기

반응식

HRID 1395609 반응식
[CH:1]([CH:4]([CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=1)[C:5]([O:7]CC)=[O:6])([CH3:3])[CH3:2].[OH-].[K+].CO>O>[CH:1]([CH:4]([CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=1)[C:5]([OH:7])=[O:6])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 53866659Ethyl 2-isopropyl-4-(4-fluorophenyl)-3-butenoate

생성물 1

HCID 538855142-Isopropyl-4-(4-fluorophenyl)-3-butenoic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of the above ester (0.46 g), potassium hydroxide (2.5 mmol), 3 ml methanol and 0.5 ml water is stirred at about 45° overnight. Methanol is removed by evaporation and then 5% NaOH-ether is added. After adjusting to about pH 3 by addition of dilute HCl, the mixture is extracted with ether. The ether phase is washed with water and brine, dried over sodium sulfate, and solvent evaporated to yield 2-isopropyl-4-(4-fluorophenyl)-3-butenoic acid.

후처리

  1. customMethanol is removed by evaporation
  2. addition5% NaOH-ether is added
  3. additionAfter adjusting to about pH 3 by addition of dilute HCl
  4. extractionthe mixture is extracted with ether
  5. washThe ether phase is washed with water and brine
  6. dry with materialdried over sodium sulfate, and solvent
  7. customevaporated

출처 및 근거

ORD 기록
ord-245ee3bfa4fb4fcea7eba4eb616a47df
출처 데이터셋
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04204071

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트