Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262556Generated: November 2, 2026

Hydrochloric Acid → HCID 86735054, compound

https://huagongshe.com/reaction/262556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorobutyryl chlorideHCID 78370—
ReactantL-ProlineHCID 145742—
ReactantHCID 178526132HCID 178526132—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 86735054HCID 86735054—

Reaction Steps

To a solution of L-proline (2.88 g.) in normal sodium hydroxide (25 ml.) chilled in an ice bath, 2 N sodium hydroxide (12.5 ml.) and 4-chlorobutyryl chloride (3.5 g.) are added. The reaction mixture is stirred at room temperature for 3.5 hours and a suspension of thiobenzoic acid (3.75 g.) and potassium carbonate (2.4 g.) in water (25 ml.) is added. After overnight stirring at room temperature, the reaction mixture is acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The organic layer is dried over magnesium sulfate and concentrated to dryness in vacuo. The residue is chromatographed on a column of silica gel with benzene-acetic acid (7:1). The fractions containing the desired material are pooled and concentrated to dryness, yield 1.35 g. A small aliquot of this material is dissolved in ethyl acetate and dicyclohexylamine is added until pH 8-10 (on a wet pH paper). The dicyclohexylamine salt crystallizes out, immediately, m.p. 159°-161°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154840
Source datasetuspto-grants-1979_05
ORD IDord-cdd2dff6bf094261a08bdcc6436f213c
Source noteuspto-grants-1979_05