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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531831Generated: November 3, 2026

1-Bromo-2-Chloroethane → HCID 21250993, compound

https://huagongshe.com/reaction/1531831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantTriethylamineHCID 8471—
Reactant4-fluoro-N-(piperidin-4-yl)benzamideHCID 4778226—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21250993HCID 21250993—

Reaction Steps

A mixture of 4-(4-fluorobenzamido)piperidine (2 g; preparation 2), triethylamine (3.75 ml) and 1-bromo-2-chloroethane (1.11 ml) in 150 ml of dry tetrahydrofuran was refluxed overnight, then further triethylamine (3.75 ml) and 1-bromo-2-chloroethane (1.11 ml) were added. The mixture was refluxed for an additional 5 hours, treated again with 3.75 ml of triethylamine and 1.11 ml of 1-bromo-2-chloroethane and refluxed overnight. The reaction mixture was concentrated to a small volume, treated with ethyl acetate (200 ml) and the mixture washed with an aqueous saturated potassium carbonate solution. The organic phase was dried over sodium sulfate and concentrated to dryness. The residue (1.3 g) was crystallized from 10 ml of diethyl ether and dried under vacuum at 50° C., to give 1.06 g of the product, m.p. 220-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200989B1
Source datasetuspto-grants-2001_03
ORD IDord-164a2a2e920f47b6b4f623242601d707
Source noteuspto-grants-2001_03