HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743836Generated: November 1, 2026
Tetrahydrothiopyran-4-one → HCID 10107310, compound
https://huagongshe.com/reaction/1743836
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrothiopyran-4-one | HCID 66173 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 22236594 | HCID 22236594 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10107310 | HCID 10107310 | 23.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012089B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-4ef3c8fc5dd041cbad809f5288198cf0 |
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| Source note | uspto-grants-2006_03 |
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