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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610412Generated: November 2, 2026

Hydrochloric Acid → HCID 86593245, compound

https://huagongshe.com/reaction/1610412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22261818HCID 22261818—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
ProductHCID 86593245HCID 8659324587.4%

Reaction Steps

To a solution of zinc chloride (12.3 g, 90.4 mmol) in diethyl ether (150 ml) was added sodium borohydride (6.85 g, 181 mmol) and the mixture was stirred at room temperature for 30 min. The insoluble material was filtered off. To the filtrate was added a solution of ethyl 3-(4-methoxyphenyl)-3-oxo-2-((4-(trifluoromethyl)phenyl)methyl)propionate (17.2 g, 45.2 mmol) in diethyl ether (50 ml) and the mixture was stirred at room temperature for 30 min. 1N Hydrochloric acid was added to the reaction solution under ice-cooling for quenching, water (200 ml) was added, and 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 silica gel column chromatography (hexane:ethyl acetate=4:1-2:1) to give ethyl (2RS,3RS)-3-hydroxy-3-(4-methoxyphenyl)-2-((4-(trifluoromethyl)phenyl)methyl)propionate (15.1 g, 87%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-e49c022e8f9f4908abf5017e333658e5
Source noteuspto-grants-2006_01