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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610438Generated: November 2, 2026

Hydrochloric Acid → HCID 22261661, compound

https://huagongshe.com/reaction/1610438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22262302HCID 22262302—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
ProductHCID 22261661HCID 2226166166.2%

Reaction Steps

To a solution of zinc chloride (9.89 g, 72.6 mmol) in diethyl ether (150 ml) was added sodium borohydride (5.49 g, 145 mmol), and the mixture was stirred at room temperature for 30 min. The insoluble material was filtered off, and a solution of ethyl 3-(6-chloro-3-pyridyl)-3-oxo-2-((4-(trifluoromethyl)phenyl)methyl)propionate (14 g, 36.3 mmol) in diethyl ether (50 ml) was added to the filtrate. The mixture was stirred at room temperature for 30 min. 1N Hydrochloric acid was added to the reaction solution under ice-cooling to quench the reaction and water (200 ml) was added. The mixture was extracted with ethyl acetate (300 ml×2). The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by medium pressure silica gel column chromatography (hexane:ethyl acetate=4:1) to give ethyl(2RS,3RS)-3-(6-chloro-3-pyridyl)-3-hydroxy-2-((4-(trifluoromethyl)phenyl)methyl)propionate (9.32 g, 66%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-6add1d1c7cdf47b38b37e796a3c86890
Source noteuspto-grants-2006_01