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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403375Generated: November 3, 2026

Pinacol → HCID 66617603, compound

https://huagongshe.com/reaction/2403375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPinacolHCID 6425—
ReactantTriisopropyl borateHCID 21531—
Reactant5-Bromo-1,2-difluoro-3-(4-methoxy-benzyloxy)-benzeneHCID 66617672—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66617603HCID 66617603—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 5-bromo-1,2-difluoro-3-(4-methoxy-benzyloxy)-benzene (0.35 g) in tetrahydrofuran (10 ml) under nitrogen was added triisopropylborate (0.29 ml). The mixture was cooled to −78° C. and 2.5M n-butyllithium solution in hexanes was added. The reaction mixture was stirred at −40° C. for 1 hour, then warmed to 20° C. and quenched with 2M hydrochloric acid (aq) (2 ml). The reaction mixture was warmed to room temperature and stirred for 1 hour. The reaction mixture was adjusted to pH 7 using saturated sodium bicarbonate solution, then partitioned between ethyl acetate and water, dried (MgSO4) and the solvents removed in vacuo to yield a crude residue (0.31 g). A mixture of this crude residue and pinacol (0.25 g) in toluene (10 ml) were stirred under reflux overnight in a Dean-Stark apparatus. The solvents were removed in vacuo, the residue was then partitioned between ethyl acetate and water, the combined organics were washed with water then brine and dried (MgSO4), the solvents were removed in vacuo to yield 2-[3,4-difluoro-5-(4-methoxy-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (0.28 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802670B2
Source datasetuspto-grants-2014_08
ORD IDord-07b1ca44b7c143e1a399d9836521cb22
Source noteuspto-grants-2014_08