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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371708Generated: October 27, 2026

Dimethylformamide → Ethyl 4-(dibenz[b,e]oxepin-11(6H)-ylidene)-1-piperidinepropionate

https://huagongshe.com/reaction/2371708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-bromopropionateHCID 68320—
Reactant4-(dibenz[b,e]oxepin-11(6H)-ylidene)piperidineHCID 9947379—
SolventWaterHCID 962—
ProductEthyl 4-(dibenz[b,e]oxepin-11(6H)-ylidene)-1-piperidinepropionateHCID 1027674885.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3.61 g of 4-(dibenz[b,e]oxepin-11(6H)-ylidene)piperidine, 2.6 g of ethyl 3-bromopropionate, 1.8 g of potassium carbonate and 25 ml of N,N-dimethylformamide was stirred at 80° C. for 2 hrs. After cooling, water was added to the reaction mixture and extracted with ether. The ether layer was washed with water and extracted with hydrochloric acid. The aqueous layer was made alkaline with potassium carbonate and extracted with ether. The ether layer was washed with water, dried and concentrated to give 4.2 g of yellowish brown liquid, which was purified by column chromatography on silica gel (eluent: chloroform) to give 3.9 g of pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05095022
Source datasetuspto-grants-1992_03
ORD IDord-1ecece786d914257a0bd871fa5431f8c
Source noteuspto-grants-1992_03