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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878763Generated: November 1, 2026

Methanol → (3,3-Dimethyl-2,3-dihydro-1-benzofuran-6-yl)methanol

https://huagongshe.com/reaction/878763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantLithium borohydrideHCID 4148881—
ReactantMethyl 3,3-dimethyl-2,3-dihydrobenzofuran-6-carboxylateHCID 58279528—
SolventTetrahydrofuranHCID 8028—
Product(3,3-Dimethyl-2,3-dihydro-1-benzofuran-6-yl)methanolHCID 68289793101.5%

Reaction Steps

To a solution of methyl 3,3-dimethyl-2,3-dihydro-1-benzofuran-6-carboxylate (44 mg, 0.21 mmol) prepared in the method of US2009/105209 in tetrahydrofuran (1.5 mL) were added lithium borohydride (23 mg, 1.07 mmol) and methanol (43 μL, 1.07 mmol) at 0° C., and the mixture was stirred at room temperature for 1 hour. To the reaction solution was added water, and the mixture was extracted with ethyl acetate twice. The organic layer was combined, washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to give the title compound (38 mg, 100%) as a colorless and clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987445B2
Source datasetuspto-grants-2015_03
ORD IDord-c33acc6ee9a742cb834f8f60b2a8b7f1
Source noteuspto-grants-2015_03