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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368132Generated: November 3, 2026

Sodium borohydride → HCID 178472331, compound

https://huagongshe.com/reaction/2368132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178472330HCID 178472330—
SolventEthanolHCID 702—
ProductHCID 178472331HCID 17847233199.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-({trans-4-[6-(cyclopropylmethoxy)-1-benzofuran-2-yl]cyclohexyl}oxy)propan-2-one (556 mg) in ethanol (10 mL) was added sodium borohydride (123 mg) under ice-cooling. The mixture was stirred at 0° C. for 1 hr and extracted with ethyl acetate and 1M hydrochloric acid. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (555 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-bacd389f5f9f421a84b7e46d0dfb5b8b
Source noteuspto-grants-2014_04