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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380091Generated: November 1, 2026

Tetrahydrofuran → HCID 18367412, compound

https://huagongshe.com/reaction/380091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 18367238HCID 18367238—
SolventEthyl AcetateHCID 8857—
ProductHCID 18367412HCID 18367412—

Reaction Steps

A mixture of 3-[3-(4,5-diphenyloxazol-2-yl)-3-hydroxy-2-(2-hydroxyethyl)propyl]-1-methoxybenzene (3.3 g) and methanesulfonyl chloride (1.8 ml) and triethylamine (4.3 ml) in THF (50 ml) was stirred at room temperature for 1 hour. The solution was diluted with ethyl acetate and washed with sat. NaHCO3 and brine, dried over MgSO4, and evaporated. The residue was dissolved in benzylamine (10 ml). After being stirred for 2 hours at 80° C., the mixture was partitioned between ether and water. The organic layer was washed with water and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to afford 1-benzyl-2-(4,5-diphenyloxazol-2-yl)-3-(3-methoxybenzyl)pyrrolidine (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300344B1
Source datasetuspto-grants-2001_10
ORD IDord-fae8a1e1d4754210b73114ebbc35a487
Source noteuspto-grants-2001_10