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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603850Generated: October 30, 2026

Epichlorohydrin → HCID 5328503, compound

https://huagongshe.com/reaction/1603850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
Reactant1-Phenyl-1H-benzimidazol-5-olHCID 667662—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 5328503HCID 5328503—

Reaction Steps

A solution of 5-hydroxy-1-phenylbenzimidazole (Example 14) (0.24 g, 1.14 mmol) 1:1 THF/DMF (5 mL) was added under nitrogen to a stirred suspension of sodium hydride (41 mg of a 60% dispersion in oil, 1.71 mmol). After 5 minutes, epichlorohydrin (98 μL, 1.26 mmol) was added, and the solution was refluxed for 4 hours. The cooled solution was partitioned between diethyl ether and water, and the extract was washed with 2N NaOH and worked up to give an oil which was chromatographed on silica gel. EtOAc/petroleum ether (1:1) eluted foreruns, while EtOAc eluted the epoxide Example 34 (0.14 g, 46%): mp (EtOAc/petroleum ether) 96-97.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990146
Source datasetuspto-grants-1999_11
ORD IDord-ce5c2d6bccd54421be09c139cfd79ee3
Source noteuspto-grants-1999_11