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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610739Generated: October 29, 2026

Sodium borohydride → HCID 86593309, compound

https://huagongshe.com/reaction/1610739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22262346HCID 22262346—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
ProductHCID 86593309HCID 8659330981%

Reaction Steps

To a suspension (60 ml) of zinc chloride (4.75 g, 34.8 mmol) in ether was added sodium borohydride (2.64 g, 69.6 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-(neopentyloxy)benzyl]-3-(3-chlorophenyl)-3-oxopropionate (2.64 g, 69.6 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=8:1, 3:1) to give ethyl (2RS,3RS)-2-[3-(neopentyloxy)benzyl]-3-(3-chlorophenyl)-3-hydroxypropionate (5.82 g, 81%) as a colorless transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-83048803da944ded947a930831609db2
Source noteuspto-grants-2006_01