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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384393Generated: November 1, 2026

Hexane → (2,3-dihydro-1H-inden-5-yl)boronic acid

https://huagongshe.com/reaction/1384393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTriethyl borateHCID 9009—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-bromo-2,3-dihydro-1H-indeneHCID 267139—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2,3-dihydro-1H-inden-5-yl)boronic acidHCID 22240187—

Reaction Conditions

Temperature-65 °C

Reaction Steps

A solution of n-butyllithium in hexane (13.2 mL of 1.6 M, 21 mmol) is added to a stirred solution of 5-bromo-indane (1.06 g, 4 mmol) in dry tetrahydrofuran (30 mL) at −75° C. under an argon atmosphere. The mixture is stirred for 30 min at −65° C., then treated with triethylborate (3.07 g, 21 mmol) and stirred for 60 min at −50° C. The resulting mixture is allowed to warm to 0° C. and then treated with a saturated aqueous solution of ammonium chloride (60 mL) and extracted with ethyl acetate (2×80 mL). The combined extracts are dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by chromatography (silica gel, 50% ethyl acetate in hexaen) and recrystallised from ethyl acetate-hexane to give indan-5-boronic acid as a colourless crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258843B1
Source datasetuspto-grants-2001_07
ORD IDord-c4c8f7320b9b4d98a1ff2559a85641af
Source noteuspto-grants-2001_07