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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040376Generated: October 31, 2026

Triisopropyl borate → 2-Chloro-5-ethoxybenzeneboronic acid

https://huagongshe.com/reaction/1040376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant1-Chloro-2-iodo-4-ethoxybenzeneHCID 58863754—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventHydrogen chloride-ethyl acetateHCID 21866389—
Product2-Chloro-5-ethoxybenzeneboronic acidHCID 2230946159%

Reaction Steps

Add, dropwise, 5.5 mL (8.8 mmol) of a 1.6N solution of butyllithium in hexane in the space of 30 min to a solution of 2.38 g (8.4 mmol) of 1-chloro-2-iodo-4-ethoxybenzene in 50 mL of anhydrous THF cooled under argon to −78° C. After 2 h at −70° C., add 1.74 g (9.2 mmol) of triisopropyl borate and stir the reaction mixture for 3 h at room temperature, then distribute in 200 mL of EtOAc/HCl aq 5N 1:1 mixture. Wash the organic phase with 50 mL of water, dry over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a DCM/methanol gradient from 0 to 10% of methanol. After concentration under reduced pressure, we obtain 990 mg of (2-chloro-5-ethoxyphenyl)boronic acid, in the form of oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552201B2
Source datasetuspto-grants-2013_10
ORD IDord-13614a87225c43048bfc859154573618
Source noteuspto-grants-2013_10