HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538630Generated: October 26, 2026
Water → 4-(Acetylthiomethyl)tetrahydropyran
https://huagongshe.com/reaction/538630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate | HCID 19077576 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 4-(Acetylthiomethyl)tetrahydropyran | HCID 59704018 | 96% |
Reaction Steps
To 224 g (0.83 mol) of toluene-4-sulfonic acid tetrahydro-pyran-4-ylmethyl ester in methyl isobutylketone (1.6 L) are added 189 g (1.66 mol) of potassium thioacetate. The suspension is stirred at 70° C. for 4.5 h. The reaction mixture is cooled to RT and water (1.8 L) is added. The organic layer is washed with 10% aq. K2CO3 solution (1.8 L) and water (1 L). The organic layer is filtered through Celite® (20 g), activated charcoal (20 g) and Na2SO4 (20 g) and the filtrate is concentrated under reduced pressure. The residual oil is azeotroped with methylcyclohexane (200 mL) and n-heptanes (250 mL) to afford 138 g of thioacetic acid S-(tetrahydro-pyran-4-ylmethyl) ester. Yield: 96%; ESI-MS: 175 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865744B1 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-bdba0048fabe40588e164281e7923365 |
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| Source note | uspto-grants-2014_10 |
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