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Formaldehyde → Ethyl alpha-(phenethyl)acrylate

HRID 983672
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HRID 983672 반응식
C([C:3]([CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([C:7](O)=O)[C:4]([OH:6])=[O:5])C.N1CCC[CH2:20][CH2:19]1.C=O>>[CH2:7]=[C:3]([CH2:10][CH2:11][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[C:4]([O:6][CH2:19][CH3:20])=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 712FormaldehydeHCID 8082PiperidineHCID 22561331Monoethyl 2-[2-(phenyl)ethyl]malonic acid

생성물 1

HCID 11117162Ethyl alpha-(phenethyl)acrylate수율 89%

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온도
57.5 °C

실험 절차

Monoethyl 2-[2-(phenyl)ethyl]malonic acid (47.2 g, 200 mole) was added to 40 mL round bottom flask fitted with a Teflon coated stirring bar. Piperidine (3 mL) and paraformaldehyde (8.4 g, 280 mmole) were added to the flask and the flask was heated to 55-60° C., until gas evolution ceased. TLC indicated that no starting material remained. The solution was worked up by removing the solvent under reduced pressure. Water (50 mL) and enough 12N HCl was added to the flask to acidify the mixture (pH>3). The mixture was extracted with ether (3×50 mL) and back extracted with brine. The solution was dried over MgSO4 and filtered. The reaction mixture was shown to be clean by NMR and TLC and used without further purification. Recovered 36.3 g material (89% yield).

후처리

  1. customfitted with a Teflon coated stirring bar
  2. customby removing the solvent under reduced pressure
  3. additionWater (50 mL) and enough 12N HCl was added to the flask
  4. extractionThe mixture was extracted with ether (3×50 mL)
  5. extractionback extracted with brine
  6. dry with materialThe solution was dried over MgSO4
  7. filtrationfiltered
  8. customused without further purification

출처 및 근거

ORD 기록
ord-8c2dc2657849450cbfd727c9ee3dd93c
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06864383B2

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