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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027239Generated: October 28, 2026

Trimethyl borate → 4-Benzyloxy-2-(trifluoromethoxy)phenylboronic acid

https://huagongshe.com/reaction/1027239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant4-(Benzyloxy)-1-bromo-2-(trifluoromethoxy)benzeneHCID 67236236—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyloxy-2-(trifluoromethoxy)phenylboronic acidHCID 86710618135.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of 4-(benzyloxy)-1-bromo-2-(trifluoromethoxy)benzene (1.8 g, 5.19 mmol) in THF (20 mL) was added butyllithium (2.5 M in THF, 2.28 mL, 5.70 mmol) at −78° C. dropwise over 10 minutes. The reaction mixture was stirred at −78° C. for 1 h, then trimethylborate (1.73 mL, 15.6 mmol) was added. The mixture was warmed to room temperature and stirred overnight. The mixture was concentrated from diethyl ether three times and the residue was dried on high vacuum to provide the title compound as a gummy solid (2.2 g, 61% pure, 83% yield). The crude material was carried on without further purification. MS (M−1)=311.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-225159859b19461c93f562a0e1dbbd20
Source noteuspto-grants-2014_05