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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52860Generated: October 28, 2026

Lithium borohydride → (2RS,3RS)-2-(3,4-dichlorobenzyl)-1,3-butanediol

https://huagongshe.com/reaction/52860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
Reactanttert-butyl (2RS,3RS)-2-(3,4-dichlorobenzyl)-3-hydroxybutanoateHCID 53695590—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(2RS,3RS)-2-(3,4-dichlorobenzyl)-1,3-butanediolHCID 1907370190%

Reaction Steps

3.0 g of the alcohol compound thus obtained was dissolved in a liquid mixture of 30 ml of ethyl ether and 30 ml of tetrahydrofuran, and 1.2 g of lithium borohydride was added thereto with stirring under cooling with ice. The mixture was stirred at room temperature for 3 hours. The reaction solution was diluted with ethyl ether, then washed with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and then the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (hexane/ethyl acetate=10/1) to obtain 2.1 g (yield: 90%) of (2RS, 3RS)-2-(3,4-dichlorobenzyl)-1,3-butanediol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616803
Source datasetuspto-grants-1997_04
ORD IDord-6f8b14c43770430a9145bc1c8e33fe1a
Source noteuspto-grants-1997_04