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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29457Generated: October 26, 2026

3-Methyl-1-benzofuran-2-carboxylic acid → 3-Methyl-2-benzofuranmethanol

https://huagongshe.com/reaction/29457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-1-benzofuran-2-carboxylic acidHCID 600591—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-2-benzofuranmethanolHCID 1024110887%

Reaction Steps

A solution of 3-methyl-benzofuran-2-carboxylic acid (2.0 g, 11.4 mmol, 1 eq) in 60 mL of THF under nitrogen was placed in water bath. Then 30 mL of BH3.THF (1.0 M in THF, 30 mmol, 2.6 eq) was added dropwise. The reaction mixture was allowed to stir at room temperature for 12 h. Then the reaction was quenched with methanol (10 mL). Solvent was removed in vacuo and the residue was subjected to column chromatography eluting with 20% ethyl acetate/hexane to give (3-methyl-benzofuran-2-yl)-methanol (1.6 g) in 87% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.2 (s, 3 H) 4.5 (d, J=5.8 Hz, 2 H) 5.3 (t, J=5.8 Hz, 1 H) 7.3 (m, 2 H) 7.5 (m, 1 H) 7.6 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-5d8efb45f78b407db502724f69cc21b4
Source noteuspto-grants-2008_09