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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089486Generated: October 30, 2026

Sodium borohydride → 2,2-Dimethyl-2,3-dihydrobenzofuran-3-ol

https://huagongshe.com/reaction/2089486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2,2-Dimethyl-1-benzofuran-3(2H)-oneHCID 12554350—
SolventMethanolHCID 887—
Product2,2-Dimethyl-2,3-dihydrobenzofuran-3-olHCID 19013020—

Reaction Steps

To a solution of 2,2-dimethyl-benzofuran-3-one (1.58 g, 9.7 mmol) in methanol (30 mL) at 0° C. is added NaBH4 (0.36 g, 9.7 mmol). The reaction is placed at room temperature and another equivalent of NaBH4 (0.36 g, 9.7 mmol) is added. After three hours the reaction is quenched with saturated aqueous NH4Cl. The reaction is concentrated to approximately ¾ of its original volume, diluted with ethyl acetate, and washed with 2N aqueous HCl, followed by brine. The organic layer is dried with Na2SO4, filtered, and concentrated. The resulting residue is purified by silica gel flash chromatography (ethyl acetate-heptane, 0:1 to 1:8) to provide 2,2-dimethyl-2,3-dihydro-benzofuran-3-ol; 1H NMR (400 MHz, CDCl3) δ ppm 1.34 (s, 3 H), 1.49 (s, 3 H), 1.96 (d, J=8.6 Hz, 1 H), 4.71 (d, J=8.6 Hz, 1 H), 6.79 (d, J=8.1 Hz, 1 H), 6.87-6.95 (m, 1 H), 7.21-7.26 (m, 1 H), 7.39 (d, J=7.3 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436035B2
Source datasetuspto-grants-2013_05
ORD IDord-93586b9da3254c46853093c323854b4d
Source noteuspto-grants-2013_05