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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091427Generated: November 2, 2026

Sodium borohydride → HCID 66778077, compound

https://huagongshe.com/reaction/2091427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66777635HCID 66777635—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66778077HCID 6677807794.3%

Reaction Steps

Cyclohexyl(5-fluoro-3-methoxy-1-benzofuran-2-yl)methanone (2.0 g) synthesized in the above-mentioned (2) was dissolved in tetrahydrofuran (15 mL) and methanol (3 mL), and sodium borohydride (90%, 0.59 g) was added to the solution under ice-cooling. The ice bath was removed, and the reaction mixture was stirred at room temperature for 1 hr then ice-cooled again, and water (2 mL) and 1N hydrochloric acid (10 mL) were carefully added to the mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give a crude product (1.9 g, quantitative) of the title object compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-6127c19184954a769debd2bdf9db20c0
Source noteuspto-grants-2013_05