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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514497Generated: October 25, 2026

2,3-Dihydro-1-benzofuran-7-carboxylic acid → (2,3-Dihydro-1-benzofuran-7-yl)methanol

https://huagongshe.com/reaction/514497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 2795014—
SolventTetrahydrofuranHCID 8028—
Product(2,3-Dihydro-1-benzofuran-7-yl)methanolHCID 279502077.3%

Reaction Steps

Added BH3 (1M in THF, 9 mL) to a solution of 2,3-dihydro-1-benzofuran-7-carboxylic acid (481 mg, 2.93 mmol) in THF (7 mL) drop wise at 0° C., thereto, the mixture was stirred at room temperature overnight. Extracted with ethyl acetate twice, and washed the organic phase with brine and dried with anhydrous Na2SO4, concentrated to give the title compound (340 mg, 77%). 1H NMR (400 MHz, CDCl3): δ 2.09 (1H, s), 3.22 (2H, t, J=8.8 Hz), 4.61 (2H, t, J=8.8 Hz), 4.67 (2H, s), 6.83 (1H, t, J=7.6 Hz), 7.08 (1H, d, J=7.2 Hz), 7.14 (1H, d, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107916B2
Source datasetuspto-grants-2015_08
ORD IDord-b276d3d559e24643a12d93e167ec99cd
Source noteuspto-grants-2015_08