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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042331Generated: November 3, 2026

Triisopropyl borate → (7-(Trifluoromethyl)benzo[b]thiophen-2-yl)boronic acid

https://huagongshe.com/reaction/2042331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantHCID 59133208HCID 59133208—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(7-(Trifluoromethyl)benzo[b]thiophen-2-yl)boronic acidHCID 57356028—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 7-trifluoromethyl-benzo[b]thiophene (0.52 g, 0.0026 mol) in THF (30 mL) at −78° C. was added 2.5 M of n-BuLi in hexane (1.4 mL). The reaction was then slowly warmed up to −30° C. over 30 min. and stirred at this temperature for 10 min prior to recooling to −78° C. and treatment with triisopropyl borate (0.7255 g, 0.0038 mol). The reaction was then slowly warmed up to 0° C. then was quenched with saturated ammonium chloride and the solvent removed in vacuo. To the residue was added aqueous sodium hydroxide (10 mL, 2N solution) followed by water (30 mL) then this mixture was extracted with DCM. The aqueous solution was acidified using dilute sulfuric acid (2N solution), filtered and the residue dried in vacuo to yield 7-trifluoromethylbenzo[b]thiophen-2-boronic acid. 1H NMR (400 MHz, MeOD) δ ppm 7.55 (1 H, t, J=7.45 Hz), 7.75 (1 H, d, J=7.07 Hz), 8.02 (1 H, s) and 8.17 (1 H, d, J=7.83 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586546B2
Source datasetuspto-grants-2013_11
ORD IDord-83cb8cafcaf64f3aaf0e6e1d30584815
Source noteuspto-grants-2013_11