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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Malonic Acid → 3-Allyl-4-hydroxy-cinnamic acid

HRID 259626
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반응식

HRID 259626 반응식
C(O[C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][C:12]=1[OH:13])[CH:8]=O)C=C.[C:14]([OH:20])(=[O:19])[CH2:15]C(O)=O.N1CC[CH2:24][CH2:23][CH2:22]1>N1C=CC=CC=1>[CH2:24]([C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][C:12]=1[OH:13])[CH:8]=[CH:15][C:14]([OH:20])=[O:19])[CH:23]=[CH2:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 867Malonic AcidHCID 8082PiperidineHCID 155743773-(Allyloxy)-4-hydroxybenzaldehyde

생성물 1

HCID 540628753-Allyl-4-hydroxy-cinnamic acid

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

48.5 g (0.27 mol) of 3-allyloxy-4-hydroxy-benzaldehyde, 104 g (1 mol) of malonic acid, 140 ml of pyridine and 4 ml of piperidine are heated to 100° C. for 2 hours, whilst stirring. The volatile constituents are distilled off under reduced pressure at 80° C. and the residue is stirred with 800 ml of water. The crystals obtained are filtered off and recrystallised from methylene chloride. 3-Allyl-4hydroxy-cinnamic acid of melting point 132°-133° C. is obtained.

후처리

  1. distillationThe volatile constituents are distilled off under reduced pressure at 80° C.
  2. stirringthe residue is stirred with 800 ml of water
  3. customThe crystals obtained
  4. filtrationare filtered off
  5. customrecrystallised from methylene chloride

출처 및 근거

ORD 기록
ord-548327931f1546e6a760d4cef79c0a34
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04038414

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