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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217156Generated: November 2, 2026

Ethanol → HCID 46907403, compound

https://huagongshe.com/reaction/2217156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 69255012HCID 69255012—
ReactantSodium tetraborohydrideHCID 131720822—
SolventWaterHCID 962—
ProductHCID 46907403HCID 4690740322%

Reaction Steps

Solid sodium tetraborohydride (654 mg, 17.2 mmol) was added in three portions at two hourly intervals to a stirred solution of 10 (971 mg, 1.8 mmol) in a mixture of anhydrous ethanol (19 mL) and anhydrous THF (37 mL) and left to stir at room temperature for 24 hours. The reaction mixture was diluted with water (50 mL) and extracted with ethyl acetate (3×50 mL). The organic layers were evaporated in vacuo. The crude product was treated with ethanol (50 mL), water (30 mL) and silica gel (18.3 g) and left to stir at room temperature for 24 hours. The reaction mixture was filtered and the product extracted with ethyl acetate (3×50 ). The organic layers were combined and washed with brine (20 mL) and dried over anhydrous magnesium sulphate. Filtration and evaporation in vacuo afforded the crude product, which was purified using flash column chromatography with a 70-50% hexane in ethyl acetate as eluent. Pure fractions were combined and evaporated in vacuo to afford the pure product 11 as a yellow powder (151 mg, 0.39 mmol, 22% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407951B2
Source datasetuspto-grants-2008_08
ORD IDord-cb6d86b940fc416398bac16c6f009c35
Source noteuspto-grants-2008_08