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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279884Generated: October 26, 2026

Benzyl Bromide → 3-(Benzyloxy)-2,2-difluoropropan-1-OL

https://huagongshe.com/reaction/2279884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2-Difluoropropane-1,3-diolHCID 95744—
Reactant4-Fluorophenylboronic acidHCID 285645—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(Benzyloxy)-2,2-difluoropropan-1-OLHCID 5846386950%

Reaction Steps

A suspension of 2,2-difluoropropane-1,3-diol (Compound 59I, 6.0 g, 53.5 mmol), 4-fluorophenylboronic acid (1.5 g, 10.7 mmol) and K2CO3 (11.0 g, 80.3 mmol) in DMF (50 mL) was treated with benzyl bromide (8.9 mL, 74.9 mmol). The reaction mixture was stirred at RT for 72 h, diluted with ethyl acetate (200 mL) and washed with water (5×100 mL). The organic layer was dried over Na2SO4, filtered and concentrated to give yellow oil which was purified by column chromatography (SiO2, 20% ethyl acetate/hexanes) to give 5 g (50%) of the desired product as an oil. 1H NMR (500 MHz, CDCl3) δ 7.38-7.34 (m, 5H), 4.70 (s, 2H), 3.89-3.88 (m, 2H), 3.77 (t, J=12.6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133224B2
Source datasetuspto-grants-2015_09
ORD IDord-f744759d3a4745b4a3e913426fd41e1d
Source noteuspto-grants-2015_09