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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291994Generated: October 31, 2026

Imidazole → HCID 70351161, compound

https://huagongshe.com/reaction/2291994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantThionyl ChlorideHCID 24386—
Reactantα-Phenyl-2-benzofuranmethanolHCID 15150176—
ReactantHCID 21277788HCID 21277788—
SolventAcetonitrileHCID 6342—
ProductHCID 70351161HCID 70351161—

Reaction Steps

To 0.08 moles of imidazole in 70 ml of acetonitrile, at the temperature of 10 C., 0.02 moles of thionylchloride are added, followed by 1 hour rest, and then 0.02 moles of (benzofuran-2-yl)phenylmethanol are added in 20 ml of acetonitrile. The reaction admixture is kept 24 hours at ambient temperature and then concentrated to dryness. The residue is taken up with ethylether, washed first with 2% sodium hydrate solution and then with water: the hydrochloride is obtained from the ethereal solutions using 5% hydrochloric acid, then an oil is obtained by alkalinization with 5% NaOH, which is extracted with ethylether. The ethereal extract is washed, made anhydrous and saturated with gaseous HCl: the precipitate thus obtained is crystallized from isopropanol: m.p. 205°-207° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04800208
Source datasetuspto-grants-1989_01
ORD IDord-7d1c411564f147e6b827747a4042f182
Source noteuspto-grants-1989_01