2-Propenoic acid, 3-phenyl- → HCID 67844477, compound

HRID 1637136Notes

Reaction equation

HRID 1637136 reaction equation
[C:1]([OH:11])(=[O:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH:12](=O)[CH2:13][CH:14]=[CH2:15].C1(N=C=NC2CCCCC2)CCCCC1>ClCCl>[C:4]1([CH:3]=[CH:2][C:1]([OH:11])=[O:10])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:15][CH2:14][CH:13]=[CH2:12]

Participants

5

Procedure

22.2 g of cinnamic acid, 12.5 g of but-3-en-1-al and 0.2 g of 4-N,N-dimethylaminopyridine were placed in 80 ml of dichloromethane. A solution of 33.05 g of dicyclohexylcarbodiimide in 80 ml of dichloromethane was added dropwise at 5°-10° C. within 120 minutes. The mixture was stirred at room temperature for a further 18 hours. Subsequently, the precipitated N,N'-dicyclohexylurea was filtered off and washed with 150 ml of dichloromethane. The dichloromethane solution was washed with 200 ml of 5% acetic acid and subsequently three times with 250 ml of water each time, filtered and dried over sodium sulphate. After concentrating the solution the residue was chromatographed on silica gel with dichloromethane. Drying in a high vacuum gave 22.1 g of but-3-ene 3-phenylacrylate as a colourless liquid.

Workup

  1. filtrationSubsequently, the precipitated N,N'-dicyclohexylurea was filtered off
  2. washwashed with 150 ml of dichloromethane
  3. washThe dichloromethane solution was washed with 200 ml of 5% acetic acid and subsequently three times with 250 ml of water each time
  4. filtrationfiltered
  5. dry with materialdried over sodium sulphate
  6. concentrationAfter concentrating the solution the residue
  7. customwas chromatographed on silica gel with dichloromethane
  8. customDrying in a high vacuum

Sources & evidence

ORD record
ord-4f811d439e114e4d84fdb607ca2f52ff
Source dataset
uspto-grants-2000_03
Patent number
USRE036625

Reaction notes

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