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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091374Generated: October 31, 2026

Sodium borohydride → HCID 66778775, compound

https://huagongshe.com/reaction/2091374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 43805642HCID 43805642—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66778775HCID 6677877598.1%

Reaction Steps

(5-Bromo-3-methyl-1-benzofuran-2-yl)(cyclohexyl)methanone (7.5 g) synthesized in the above-mentioned (1) was dissolved in tetrahydrofuran (100 mL) and methanol (15 mL), and sodium borohydride (90%, 1.9 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 (10 mL) and 1N hydrochloric acid (50 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 (7.4 g, quantitative) of the title object compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-5a66b02c74f14ee6acbbf2bbc7a65843
Source noteuspto-grants-2013_05