Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171681Generated: November 4, 2026

Sodium borohydride → HCID 23138777, compound

https://huagongshe.com/reaction/1171681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23139082HCID 23139082—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23138777HCID 2313877729%

Reaction Steps

Sodium borohydride (400 mg) was added to a solution of (E)-3-{[2-(methoxycarbonylmethyl)-2H-tetrazol-5-yl]methylidene}-1-(triphenylmethyl)piperidin-4-one (5.18 g) in tetrahydrofuran (100 ml) at 0° C. After the mixture was stirred at the same temperature for 2 hours, the reaction was quenched by addition of a saturated aqueous ammonium chloride solution. The mixture was extracted with ethyl acetate, and the extract was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The extract was concentrated under reduced pressure, and the objective material that emerged was collected by filtration. The mother liquor was concentrated and the residue was purified by silica gel chromatography using hexane, ethyl acetate, and dichloromethane (1:1:1) as an eluent to afford an additional amount of the title compound as a colourless amorphous solid. Total amount: 1.5 g, total yield: 29%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-bcf0092f9c774e33b26c6f43bf2ee034
Source noteuspto-grants-2010_11