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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243574Generated: October 30, 2026

Triisopropyl borate → 5-Ethoxymethoxy-benzofuran-2-boronic acid

https://huagongshe.com/reaction/243574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant5-Ethoxymethoxy-benzofuranHCID 59227450—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-Ethoxymethoxy-benzofuran-2-boronic acidHCID 4618397052.2%

Reaction Steps

To a stirred solution of 5-ethoxymethoxy-benzofuran (3) (265 mg, 1.38 mmol) in THF (5 mL) at −78° C., n-butyllithium (2.5M solution in hexane, 0.56 mL, 1.44 mmol) was added drop wise. After the reaction mixture was stirred for 1 hour, triisopropylborate (0.635 mL, 2.76 mmol) was added slowly and the stirring was continued for additional 20 minutes at −78° C. The reaction mixture was quenched with saturated ammonium chloride solution (10 mL) and was allowed to warm to room temperature. Water (10 mL) was added and the resulting mixture was extracted in diethyl ether (2×50 mL). The combined extracts were washed with brine, dried over MgSO4, and concentrated under reduced pressure. Purification of the crude product by recrystallization from ethyl acetate and hexane afforded the desired compound (4) (170 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653274B2
Source datasetuspto-grants-2014_02
ORD IDord-da2f1a1fca644f81bfceeb3a2daa8ac4
Source noteuspto-grants-2014_02