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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993254Generated: November 3, 2026

Triisopropyl borate → (7-Chloro-1-benzothiophen-2-yl)boronic acid

https://huagongshe.com/reaction/1993254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Chloro-1-benzothiopheneHCID 11062812—
SolventTetrahydrofuranHCID 8028—
Product(7-Chloro-1-benzothiophen-2-yl)boronic acidHCID 5099045196.2%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 7-chlorobenzo[b]thiophene (1.0 g, 5.92 mmol) in THF (25 mL) at −78° C. was added nbutyllithium (7.41 mL, 11.8 mmol, 1.6 M solution). The reaction was allowed to warm to −30° C. then was cooled back to −78° C. and triisopropyl borate (2.23 g, 11.8 mmol) was added. The mixture was allowed to warm to 0° C., saturated ammonium chloride added and the organic phase separated off and concentrated in vacuo. To the residue was added aqueous sodium hydroxide (10 mL, 2N solution) followed by water (30 mL) and the mixture was washed with DCM. The aqueous phase was acidified with 2N sulfuric acid, and the resulting precipitate isolated by filtration and dried under vacuum to yield 7-chlorobenzo[b]thiophene-2-boronic acid (1.21 g, 96%) as white solid. 1H NMR (400 MHz, CDCl3) δ=7.41 (t, J=7.70 Hz, 1H), 7.50 (d, J=7.70 Hz, 1H), 7.91 (d, J=7.70 Hz, 1H), 8.03 (s, 1H), 8.63 (s, 2H); MS (ES+): m/z 211.86 [M+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07651687B2
Source datasetuspto-grants-2010_01
ORD IDord-84e8f5c7907e47baa69d752c1c0ada91
Source noteuspto-grants-2010_01