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

Methyl beta-benzoyl-alpha-methoxypropionate → Methyl-4-oxo-4-phenyl-2-butenoate

HRID 982181
노트
인쇄 미리보기

반응식

HRID 982181 반응식
[C:1]([CH2:9][CH:10](OC)[C:11]([O:13][CH3:14])=[O:12])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C1(C)C=CC=CC=1>[C:1](/[CH:9]=[CH:10]/[C:11]([O:13][CH3:14])=[O:12])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 13934019Methyl beta-benzoyl-alpha-methoxypropionate

생성물 1

HCID 1484788Methyl-4-oxo-4-phenyl-2-butenoate수율 89.8%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
80 °C

실험 절차

A mixture of 268 mg of methyl β-benzoyl-α-methoxypropionate, 150 mg of paratoluenesulfonic acid monohydrate and 5 ml of toluene was stirred at 80° C. for 1 hour. A pressure was reduced with an aspirator and a total amount of the resultant was reduced to 1/2 by concentration. The resultant was stirred at 80° C. for 20 minutes and was left for cooling. The reaction mixture was distributed between ethyl acetate and water and the ethyl acetate layer was washed with a saturated solution of NaHCO3 and then with water, and was dried with anhydrous magnesium sulfate. The solvent was distilled away to give 206 mg of methyl trans-β-benzoylacrylate as a yellow oil.

후처리

  1. concentrationa total amount of the resultant was reduced to 1/2 by concentration
  2. stirringThe resultant was stirred at 80° C. for 20 minutes
  3. waitwas left
  4. temperaturefor cooling
  5. washthe ethyl acetate layer was washed with a saturated solution of NaHCO3
  6. dry with materialwith water, and was dried with anhydrous magnesium sulfate
  7. distillationThe solvent was distilled away

출처 및 근거

ORD 기록
ord-90951170d11443ccbee000e8a444a528
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04994600

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트