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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091389Generated: October 31, 2026

Sodium borohydride → HCID 66778107, compound

https://huagongshe.com/reaction/2091389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66777760HCID 66777760—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66778107HCID 6677810750%

Reaction Steps

1-(5-Cyclopropyl-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-one (0.80 g) synthesized in the above-mentioned (1) was dissolved in tetrahydrofuran (10 mL) and methanol (1 mL), and sodium borohydride (90%, 0.34 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 (1 mL) and 1N hydrochloric acid (5 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 the title object compound (0.4 g, 50%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-8dac8f3adcd84a27a838827c80783529
Source noteuspto-grants-2013_05