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

Water → 2-(4-Methoxyphenyl)prop-2-enoic acid

HRID 1859308
노트
인쇄 미리보기

반응식

HRID 1859308 반응식
O[C:2]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1)([CH3:6])[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.O>O1CCOCC1>[CH3:14][O:13][C:10]1[CH:9]=[CH:8][C:7]([C:2](=[CH2:6])[C:3]([OH:5])=[O:4])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 1118Sulfuric AcidHCID 131581022-Hydroxy-2-(4-methoxyphenyl)propanoic acid

생성물 1

HCID 145737872-(4-Methoxyphenyl)prop-2-enoic acid수율 78.2%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

2-Hydroxy-2-(4-methoxyphenyl)propionic acid (35 g, 178 mmol) was dissolved in dioxane (700 ml) and concentrated sulfuric acid (60 ml) was added thereto. The reaction mixture was refluxed for 2 hours under heating. The reaction solution was cooled and, after adding water, extracted with ethyl acetate. The organic layer was washed with saturated sodium thiosulfate solution and water, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 24.8 g (yield: 72%) of the title compound as a brown solid.

후처리

  1. temperatureThe reaction mixture was refluxed for 2 hours
  2. temperatureunder heating
  3. temperatureThe reaction solution was cooled
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with saturated sodium thiosulfate solution and water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-682fd67c9479434aa8ebc41887bd4154
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06153768

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트