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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743836Generated: November 1, 2026

Tetrahydrothiopyran-4-one → HCID 10107310, compound

https://huagongshe.com/reaction/1743836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrothiopyran-4-oneHCID 66173—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 22236594HCID 22236594—
Solvent1-PropanolHCID 1031—
SolventEthyl AcetateHCID 8857—
ProductHCID 10107310HCID 1010731023.6%

Reaction Steps

To a solution of 4-methyl-3,4,5,6-tetrahydro-2H-benzo[e][1,4]diazocin-1-ylamine (1.50 g, 8.1 mmole) in 1-propanol (100 mL) was added tetrahydro-thiopyran-4-one (5.0 g, 43 mmole), followed by p-toluenesulfonic acid monohydrate (3.2 g, 16.8 mmole), and the resulting reaction mixture was refluxed for 40 hours. The reaction mixture was cooled to room temperature and solvent removed in vacuo to produce a brown residue. The residue was diluted with ethyl acetate (300 mL) and washed with saturated aqueous sodium bicarbonate (150 mL), saturated aqueous sodium chloride (150 mL), dried (sodium sulfate) and concentrated in vacuo. Purification by flash column chromatography (silica gel, ethyl acetate:hexanes 1:1) provided 0.52 g of the title compound as an off-white solid, mp 123-125° C., with a trace of ethyl acetate. MS (ESI) m/z 273 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-4ef3c8fc5dd041cbad809f5288198cf0
Source noteuspto-grants-2006_03