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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475791Generated: November 3, 2026

Tetrahydrofuran → 3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic Acid

https://huagongshe.com/reaction/1475791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriisopropyl borateHCID 21531—
Reactant(3-Bromophenethoxy)(tert-butyl)dimethylsilaneHCID 11515183—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventHeptaneHCID 8900—
Product3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic AcidHCID 58845136—

Reaction Conditions

Temperature-70 °C

Reaction Steps

50.0 g of [2-(3-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane was dissolved using 500 ml of anhydrous THF and 64.6 ml of a 2.7M solution of n-butyllithium in n-heptane added dropwise at −70° C. The reaction mixture was then stirred at −70° C. for 1 h. 40.2 ml of triisopropylborate was then added dropwise at −70° C. and stirring was continued for 30 minutes at −70° C. The mixture was then allowed to warm to −20° C. and 500 ml of water added. The reaction mixture was then allowed to warm to room temperature and extracted three times using 300 ml of CH2Cl2 each. The organic layer was then dried using MgSO4 and evaporated to yield 43.6 g of the title compound, used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018383B2
Source datasetuspto-grants-2015_04
ORD IDord-a30b4bdf301c4ec38f699ae65e041a7a
Source noteuspto-grants-2015_04