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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783193Generated: November 1, 2026

Sodium borohydride → tert-Butyl (1S,2S)-3-bromo-1-(3,5-difluorobenzyl)-2-hydroxypropylcarbamate

https://huagongshe.com/reaction/1783193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57484758HCID 57484758—
SolventEthyl acetate hexaneHCID 21226206—
Producttert-Butyl (1S,2S)-3-bromo-1-(3,5-difluorobenzyl)-2-hydroxypropylcarbamateHCID 57487171—

Reaction Steps

Sodium borohydride (1.32 g, 34.9 mmole, 1.1 eq.) is added to tert-Butyl (1S)-3-bromo-1-(3,5-difluorobenzyl)-2-oxopropylcarbamate (III, EXAMPLE 1, 12 g, 31.75 mmole) dissolved in absolute alcohol (500 mL) at −78 degrees C. The reaction mixture is stirred for 0.5 hour and monitored by TLC (ethyl acetate/hexane, 20/80; Rf=0.2). The mixture is quenched with water (10 mL) and the solvent removed under reduced pressure with heat (not exceeding 30 degrees C.) to dryness. The solid is partitioned between dichloromethane and water, washed with saline, dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure to give the title compound, TLC (ethyl acetate/hexane, 20/80) Rf=0.2; MS (MH+)=381.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498436B2
Source datasetuspto-grants-2009_03
ORD IDord-cb684f35d1024cdfb4817d3c7b9e6d8d
Source noteuspto-grants-2009_03