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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377400Generated: October 27, 2026

Triisopropyl borate → (6-Methoxy-1-benzothiophen-2-yl)boronic acid

https://huagongshe.com/reaction/377400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant6-Methoxy-1-benzothiopheneHCID 13634237—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(6-Methoxy-1-benzothiophen-2-yl)boronic acidHCID 1056027671%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-methoxybenzo[b]thiophene (Graham, S. L., et al. J. Med. Chem. 1989, 32, 2548-2554)(18.13 g, 0.111 mol) in 150 mL of anhydrous THF at -60° C. was added n-BuLi (76.2 mL, 0.122 mol, 1.6 M solution in hexanes), dropwise via syringe. After stirring for 30 min, triisopropyl borate (28.2 mL, 0.122 mol) was introduced via syringe. The resulting mixture was allowed to gradually warm to 0° C. and then partitioned between 1.0 N HCl and EtOAc (300 mL each). The layers were separated, and the organic phase was dried over Na2SO4. Concentration in vacuo produced a white solid that was triturated from Et2O/hexanes. Filtration provided 16.4 g (71%) of 6-methoxybenzo[b]thiophene-2-boronic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025382
Source datasetuspto-grants-2000_02
ORD IDord-17136e36bfcc45079fd2cbde0bc8509a
Source noteuspto-grants-2000_02