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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030266Generated: November 4, 2026

Benzofuran-2-carboxylic acid → 1-Benzofuran-2-Ylmethanol

https://huagongshe.com/reaction/1030266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzofuran-2-carboxylic acidHCID 10331—
ReactantDiboronHCID 6328200—
SolventTetrahydrofuranHCID 8028—
Product1-Benzofuran-2-YlmethanolHCID 277626378.5%

Reaction Steps

1 Molar diborane in tetrahydrofuran (61.6 mL, 61.6 mmol) was added dropwise over 10 minutes to a stirred solution of benzofuran-2-carboxylic acid (5.00 g, 30.8 mmol) in tetrahydrofuran (50 mL) at 0° C. Stirring was continued at 0° C. for 30 minutes, then at room temperature for 18 hours. The reaction mixture was quenched carefully by slow addition of 1:1 THF/H2O, and extracted with ether. The organic extracts were dried (MgSO4) and concentrated to afford 3.58 g (78%) of product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104892
Source datasetuspto-grants-1992_04
ORD IDord-bafb03749d234d408fe0f661c739b440
Source noteuspto-grants-1992_04