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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610771Generated: October 31, 2026

Sodium borohydride → HCID 86593315, compound

https://huagongshe.com/reaction/1610771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22262034HCID 22262034—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
ProductHCID 86593315HCID 8659331580%

Reaction Steps

To a suspension (70 ml) of zinc chloride (4.94 g, 36.2 mmol) in ether was added sodium borohydride (2.74 g, 72.4 mmol) at room temperature, and the mixture was stirred as it was for 2 hrs. Insoluble material was filtered off. To the filtrate was added a solution of ethyl 3-(3-chlorophenyl)-2-[4-(1,1-difluoro-2,2-dimethylpropyl)benzyl]-3-oxopropionate (7.59 g, 18.1 mmol) in ether (50 ml), and the mixture was stirred at room temperature for 1 hr. The reaction was quenched with 1N hydrochloric acid, and the mixture was diluted with ethyl acetate, washed with water and saturated brine. The mixture was dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1, 10:1, 5:1) to give ethyl (2RS,3RS)-3-(3-chlorophenyl)-3-hydroxy-2-[4-(1,1-difluoro-2,2-dimethylpropyl)benzyl]propionate (6.12 g, 80%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-7035febfdad046ef90c20b012f11262d
Source noteuspto-grants-2006_01