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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881888Generated: October 26, 2026

Tetrahydrofuran → HCID 59331512, compound

https://huagongshe.com/reaction/1881888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant5-(1-Hydroxyethyl)-1,3-thiazole-2-carbaldehydeHCID 59331383—
Reactant4-[4-(methylsulfonyl)phenyl]-5-(tetrahydro-2H-pyran-4-yl)pent-1-en-3-oneHCID 68433769—
Catalyst3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chlorideHCID 2833352—
SolventEthanolHCID 702—
ProductHCID 59331512HCID 5933151276.6%

Reaction Steps

A mixture of 4-[4-(methylsulfonyl)phenyl]-5-(tetrahydro-2H-pyran-4-yl)pent-1-en-3-one (0.50 g), 5-(1-hydroxyethyl)-1,3-thiazole-2-carbaldehyde (0.28 g), 3-benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium chloride (43 mg), triethylamine (0.09 mL), tetrahydrofuran (6 mL) and ethanol (6 mL) was stirred with heating under reflux for 2 hr. The reaction mixture was concentrated, the residue was subjected to basic silica gel column chromatography, and eluted with ethyl acetate, and the fraction was concentrated. The residue was subjected to silica gel column chromatography, and the title compound (0.57 g, yield 75%) was obtained as a colorless oil from a fraction eluted with ethyl acetate. MS: 480 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-8d569434de1542b8ab4276944c0a7c38
Source noteuspto-grants-2012_11