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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445872Generated: October 29, 2026

Hydrochloric Acid → (5,6-difluoro-2,2-dimethyl-3H-benzofuran-7-yl)methanol

https://huagongshe.com/reaction/445872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant5,6-difluoro-2,2-dimethyl-3H-benzofuran-7-carboxylic acidHCID 58566306—
Product(5,6-difluoro-2,2-dimethyl-3H-benzofuran-7-yl)methanolHCID 5856659157%

Reaction Steps

To 5,6-difluoro-2,2-dimethyl-3H-benzofuran-7-carboxylic acid (735) (0.75 g, 3.29 mmol) was added 1.0 M of borane tetrahydrofuran complex solution (12 mL), and the mixture was stirred at room temperature overnight. The reaction was cooled to 0° C., acidified with 5 N HCl to pH 1, and then neutralized to pH 8 with 5 N NaOH. The mixture was extracted with EtOAc (80 mL×3) and the combined organic phase was washed with water (50 mL), dried over anhydrous sodium sulfate, and the solvent removed in vacuo. The product was purified by prep HPLC to yield (5,6-difluoro-2,2-dimethyl-3H-benzofuran-7-yl)methanol (736) (0.4 g, 57%). 1H NMR (400 MHz, DMSO-d6) δ 7.18 (t, J=9.0 Hz, 1H), 4.38 (s, 2H), 2.97 (s, 2H), 1.40 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476308B2
Source datasetuspto-grants-2013_07
ORD IDord-d2581b0d7ab541d5aa6944cb3fcb08a3
Source noteuspto-grants-2013_07