Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981321Generated: October 31, 2026

Allyl bromide → Methyl-1-[(2-chlorophenyl)methyl]-4-oxo-3-(2-propenyl)-3-piperidine carboxylate

https://huagongshe.com/reaction/981321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantMethyl 1-(2-chlorobenzyl)-4-oxo-3-piperidinecarboxylateHCID 12414560—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductMethyl-1-[(2-chlorophenyl)methyl]-4-oxo-3-(2-propenyl)-3-piperidine carboxylateHCID 20071978—

Reaction Conditions

Temperature30 °C

Reaction Steps

14.60 g (51.8 mmol) of methyl-1-[(2-chlorophenyl)methyl]-4-oxo-3-piperidine carboxylate was dissolved in 40 ml of tertbutanol and warmed to 30° C. Within 2 minutes 6.57 g (58.4 mmol) of potassium tert-butylate in 45 ml of tert-butanol was added. After 15 minutes of stirring, 25 ml of tert-butanol was added once more. Then 6.34 g (51.4 mmol) of allylbromide was added within 10 minutes and stirred for 2 more hours at 30° to 35° C. The reaction mixture was concentrated by evaporation and 70 ml of water and 70 ml of ether were added to the residue. The organic phase was washed with 50 ml of sodium sulfate solution, dried on magnesium sulfate and concentrated by evaporation. The yield was 40.68 g of methyl1-[(2-chlorophenyl)methyl]-4-oxo-3-(2-propenyl)-3-piperidine carboxylate, which equals 88.1 percent. Data concerning the compound was:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990618
Source datasetuspto-grants-1991_02
ORD IDord-5262d3a87f91438fb60ee5fab7506f85
Source noteuspto-grants-1991_02