HCID 86600459, compound → 3-Phenylprop-2-enoyl chloride
Reaction equation
N1CC1.[C:4]([Cl:14])(=[O:13])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(O)(=O)C>[C:4]([Cl:14])(=[O:13])[CH:5]=[CH:6][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
As further shown in FIG. 3, the cinnamoyl chloride aziridine intermediate was dissolved in aqueous acetic acid at 0° C., stirred at this temperature for 10 h and worked up as usual. Purification of the crude mixture by column chromatography and crystallization afforded the open chain cinnamoyl chloride intermediate.
Workup
- customPurification of the crude mixture
- customby column chromatography and crystallization
Sources & evidence
- ORD record
- ord-b617d0d5d762468ea81aa41c201e3b0c
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585986B2
Reaction notes
Loading…