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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419463Generated: November 1, 2026

Pyridine → 1-Chloroethyl Hexyl Carbonate

https://huagongshe.com/reaction/1419463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-HexanolHCID 8103—
ReactantEthyl AcetateHCID 8857—
Reactant1-Chloroethyl chloroformateHCID 521305—
SolventDichloromethaneHCID 6344—
Product1-Chloroethyl Hexyl CarbonateHCID 1350663791%

Reaction Steps

A mixture solution of 3.130 g of n-hexanol [Compound (10)] and 2.42 g of pyridine in 30 ml of dry dichloromethane was cooled to -78° C. To this mixture solution was added dropwise a solution of 4.289 g of 1-chloroethylchloroformate in 15 ml of dry dichloromethane for 1 hour. Then, the reaction mixture was stirred for 1.5 hour under ice-cooling and for 15 hours at room temperature. After the reaction, ethyl acetate was added to the reaction mixture. The organic layer was washed with 1N--HCl, saturated sodium bicarbonate aqueous solution and saturated saline solution respectively, and dried over magnesium sulfate. The solvent was removed under reduced pressure and the resulting residue was purified by silica gel column chromatography (hexane: chloroform=3:1) to give 5.697 g (91%) of 1-(n-hexyloxycarbonyloxy)ethyl-chloride [Compound (11)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886172
Source datasetuspto-grants-1999_03
ORD IDord-8cbc8ab8bb1d40bc9aa9f5e5ac93acf2
Source noteuspto-grants-1999_03