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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53336Generated: October 29, 2026

Hydrochloric Acid → HCID 19962351, compound

https://huagongshe.com/reaction/53336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
Reactant3-[2-[(4-Chlorophenyl)sulphonylamino]ethyl]-5-(4-fluorobenzoyl)benzenepropanoic acidHCID 19962368—
SolventEthanolHCID 702—
ProductHCID 19962351HCID 1996235171.7%

Reaction Steps

Sodium borohydride (0.077 g) was added portionwise to a suspension of 3-[2-[(4-chlorophenyl)sulphonylamino]ethyl]-5-(4-fluorobenzoyl)benzenepropanoic acid (0.50 g) in ethanol (12 ml), and the resulting solution was stirred at room temperature for 18 hours. 2N hydrochloric acid (5 ml) was added dropwise followed by ethyl acetate (50 ml), and the mixture was stirred for 1 hour. The organic layer was separated, washed with water and dried (MgSO4). The solvent was evaporated and the residue was chromatographed on silica gel. The column was eluted with hexane/ethyl acetate (5:1), followed by hexane/ethyl acetate/acetic acid (50:50:1), gradually increasing the polarity to give a ratio of 10:90:1. The product fractions were combined and evaporated to give the title compound as a gum (0.36 g), Rf 0.45 (SS 15). Found: C,58.58; H,4.71; N,2.65. C24H23ClFNO5S requires C,58.59; H,4.71; N,2.85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618941
Source datasetuspto-grants-1997_04
ORD IDord-a614f5cea31c4cddabb873dd7a93c038
Source noteuspto-grants-1997_04