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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767210Generated: October 31, 2026

Hydrochloric Acid → 2-(2-Benzyloxy-5-chlorophenyl)cyclopentene-1-boronic Acid

https://huagongshe.com/reaction/1767210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant1-Bromo-2-(2-benzyloxy-5-chlorophenyl)cyclopenteneHCID 21112900—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Benzyloxy-5-chlorophenyl)cyclopentene-1-boronic AcidHCID 2111291258%

Reaction Steps

A solution of n-butyllithium (0.73 ml, 1.6M in hexanes, 1.17 mmol) was added to a solution of 1-bromo-2-(2-benzyloxy-5-chlorophenyl)cyclopentene (424 mg, 1.17 mmol) in anhydrous tetrahydrofuran (12 ml) at −78° C. under nitrogen. The resulting solution was stirred for 15 minutes and triisopropyl borate (440 mg, 2.34 mmol) was added. The mixture was allowed to warm to room temperature, 1M hydrochloric acid (20 ml) was added and stirred vigorously for 15 minutes. After diluting with ether the organic phase was dried (magnesium sulphate), evaporated and purified by chromatography on silica (1:4 ethyl acetate/iso-hexane) to give the title compound as a white solid (214 mg, 58%). LC/MS: Rt 3.4, [2 MH−] 637.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232821B2
Source datasetuspto-grants-2007_06
ORD IDord-42cf77559e0e4c269ab81e6672b945c7
Source noteuspto-grants-2007_06