Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41664Generated: October 25, 2026

Sodium hydride → HCID 87499859, compound

https://huagongshe.com/reaction/41664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant[2-(4-Chlorophenyl)selenazol-5-yl]methanolHCID 59562443—
Reactant5-Chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 68567844—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87499859HCID 8749985977.8%

Reaction Steps

To a solution of [2-(4-chlorophenyl)selenazol-5-yl]methanol (300 mg, 1.1 mmol) in dry tetrahydrofuran (5 ml) is added, in one portion, sodium hydride (60% dispersion in mineral oil, 44 mg, 1.1 mmol). The reaction mixture is stirred for 5 minutes at room temperature and 5-chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (203 mg, 1.1 mmol) is added in one-portion. The reaction mixture is stirred at room temperature overnight. Silica gel is added to the crude reaction mixture, the solvent is evaporated under reduced pressure and the residue is purified by flash chromatography on silica gel to give 5-[2-(4-chloro-phenyl)-selenazol-5-ylmethoxy]-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (360 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530667B2
Source datasetuspto-grants-2013_09
ORD IDord-24f0947d47314984892ce7c6d027e7fb
Source noteuspto-grants-2013_09