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

4-Formylcinnamic acid dimethyl acetal → 3-(4-Formylphenyl)propanoic acid

HRID 918084
노트
인쇄 미리보기

반응식

HRID 918084 반응식
C[O:2][C:3](OC)([OH:14])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]=[O:13])=[CH:8][CH:7]=1>O1CCOCC1.[Pd]>[CH:12]([C:9]1[CH:10]=[CH:11][C:6]([CH2:5][CH2:4][C:3]([OH:14])=[O:2])=[CH:7][CH:8]=1)=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 865896714-Formylcinnamic acid dimethyl acetal

생성물 1

HCID 198252413-(4-Formylphenyl)propanoic acid수율 81.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 312751,4-Dioxane용매

실험 절차

A solution of 16.7 g of 4-formylcinnamic acid dimethyl acetal in 200 ml of dioxane was hydrogenated in the presence of 1 g of 5% palladium-on-carbon at room temperature and atmospheric pressure. After about 61/2 hrs., the theoretical volume of hydrogen was consumed and the uptake ceased. The reaction mixture was filtered through Celite and the filter cake was washed with 300 ml of dioxane. The filtrate was concentrated to a final volume of 200 ml, 200 ml of 1N hydrochloric acid was added, the solution was stirred at room temperature for 4 hrs. and then evaporated to dryness. The residue was dissolved in 700 ml of methylene chloride, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated to a final volume of 100 ml and the solution was allowed to stand at 0° for 16 hrs. The precipitate was collected, washed with 1:1 methylene chloride-petroleum ether and dried at 55° for 4 hrs. under vacuum to give 10.9 g (81%) of 4-formyldihydrocinnamic acid as colorless crystals, m.p. 134°-138°.

후처리

  1. custom2 hrs
  2. custom, the theoretical volume of hydrogen was consumed
  3. filtrationThe reaction mixture was filtered through Celite
  4. washthe filter cake was washed with 300 ml of dioxane
  5. concentrationThe filtrate was concentrated to a final volume of 200 ml, 200 ml of 1N hydrochloric acid
  6. additionwas added
  7. customand then evaporated to dryness
  8. dissolutionThe residue was dissolved in 700 ml of methylene chloride
  9. dry with materialdried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. concentrationThe filtrate was concentrated to a final volume of 100 ml
  12. waitto stand at 0° for 16 hrs
  13. customThe precipitate was collected
  14. washwashed with 1:1 methylene chloride-petroleum ether
  15. customdried at 55° for 4 hrs

출처 및 근거

ORD 기록
ord-c49c018fb86f44f38582e36473159d02
출처 데이터셋
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03969373

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트