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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610747Generated: November 2, 2026

Sodium borohydride → HCID 86593310, compound

https://huagongshe.com/reaction/1610747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22261940HCID 22261940—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
ProductHCID 86593310HCID 8659331084.1%

Reaction Steps

To a suspension (50 ml) of zinc chloride (3.60 g, 26.4 mmol) in ether was added sodium borohydride (2.0 g, 52.8 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 2-[3-(tert-butyl)benzyl]-3-(3-chlorophenyl)-3-oxopropionate (4.91 g, 13.2 mmol) in ether (40 ml), and the mixture was stirred at room temperature for 1 hr. The reaction was quenched with 1N hydrochloric acid. The mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1, 3:1) to give ethyl (2RS,3RS)-2-[3-(tert-butyl)benzyl]-3-(3-chlorophenyl)-3-hydroxypropionate (4.16 g, 82%) as a colorless transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-c5f6a50bbf9c47e393a7a6f010ea6aa3
Source noteuspto-grants-2006_01