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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534170Generated: November 3, 2026

Hydrochloric Acid → Ethyl 4-chlorobutyrate

https://huagongshe.com/reaction/1534170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantGamma-ButyrolactoneHCID 7302—
ReactantSodium HydroxideHCID 14798—
SolventTolueneHCID 1140—
ProductEthyl 4-chlorobutyrateHCID 1847485%

Reaction Conditions

Temperature100 °C

Reaction Steps

51.7 kg (0.6 kmol) of gamma-butyrolactone (100 percent) was placed in an enamel pressure agitator. The closed system was heated to 100° C. with good agitation, and starting from 60° C. a total of about 26.5 kg (0.72 kmol) of HCl was pressed on. The temperature and pressure quickly rose, caused by the exothermia. The addition of HCl and heat output were regulated so that the reaction could be performed isothermally at 100° C. and isobarically at 11 bars of pressure. Addition was continued until no more HCl was absorbed (about 5 to 6 hours). Then it was cooled to 20° C. and the residual HCl was discharged. Then 62.3 kg (1.35 kmol) of ethanol was added to the reaction solution. Then 2 kg (0.055 kmol) of HCl was again pressed on. It was heated to 100° C. and kept at this temperature for 2 hours (pressure was 6 bars) and then cooled to 20 ° C. The solution was then mixed with 92 kg of toluene and made basic with 23 kg of aqueous NaOH (30 percent) (pH 8 to 8.5). The phases were separated and the organic phase was washed with 26 kg of water. The combined water phases were again extracted with 46 kg of toluene. The organic phase was distilled. Thus, toluene, ethanol and water were separated. 87 kg of crude gamma-chlorobutyric acid ethyl ester (content 88 percent) remained as still residue, which could be used directly in the following step. The yield was 85 percent, relative to the gamma-butyrolactone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087745
Source datasetuspto-grants-1992_02
ORD IDord-f9a8918e796344f5b9a35c4e8696ca9f
Source noteuspto-grants-1992_02