Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717995Generated: October 25, 2026

Trimethyl borate → (6-Phenyldibenzo[b,d]furan-4-yl)boronic acid

https://huagongshe.com/reaction/717995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantAmmonium HydroxideHCID 14923—
Reactant4-PhenyldibenzofuranHCID 6425750—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(6-Phenyldibenzo[b,d]furan-4-yl)boronic acidHCID 8955692685%

Reaction Steps

n-Butyllithium (13.51 mL, 33.8 mmol) was added dropwise to 4-phenyldibenzo[b,d]furan (3.3 g, 13.51 mmol) in 80 mL dry THF at −78° C. This reaction mixture was allowed to stir at room temperature for 5 hours and then cooled to −78° C. again. Trimethyl borate (4.52 mL, 40.5 mmol) was added slowly to the reaction. The reaction mixture was allowed to warm up to room temperature gradually over night with stirring. The mixture was poured into 50 mL of NH4OH solution with ice. The aqueous mixture was extracted with 3×80 mL ethyl acetate and dried over sodium sulfate, and the organic layer was evaporated to get yield 3.3 g (85%) product, which was used without purification and was confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193745B2
Source datasetuspto-grants-2015_11
ORD IDord-d772e11d94504c63bfd97bfe1f6ec880
Source noteuspto-grants-2015_11