1-Chloroethyl chloroformate → HCID 86615853, compound
Reaction equation
C([N:8]1[CH2:13][CH2:12]/[C:11](=[CH:14]\[C:15]([O:17][CH2:18][CH3:19])=[O:16])/[CH:10]([CH3:20])[CH2:9]1)C1C=CC=CC=1.ClC(OC(Cl)C)=O>>[CH3:20][CH:10]1[CH2:9][NH:8][CH2:13][CH2:12]/[C:11]/1=[CH:14]\[C:15]([O:17][CH2:18][CH3:19])=[O:16]Participants
3
Procedure
A mixture of ethyl (2E)-(1-benzyl-3-methylpiperidine-4-ylidene)acetate, 1-chloroethyl chloroformate and 1,2-dicholoroethane was stirred for 30 minutes heated to reflux and concentrated under reduced pressure. The residue was dissolved in EtOH and stirred for 10 minutes heated to reflux to give ethyl (2E)-(3-methylpiperidine-4-ylidene)acetate.
Workup
- temperatureheated
- temperatureto reflux
- concentrationconcentrated under reduced pressure
- dissolutionThe residue was dissolved in EtOH
- stirringstirred for 10 minutes
- temperatureheated
- temperatureto reflux
Sources & evidence
- ORD record
- ord-15c348654bd0412f8dbf9bc983dfcf83
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557112B2
Reaction notes
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