HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386863Generated: October 25, 2026
Tetrahydro-2H-pyran-4-yl 4-methylbenzenesulfonate → S-Tetrahydro-2H-pyran-4-YL ethanethioate
https://huagongshe.com/reaction/386863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydro-2H-pyran-4-yl 4-methylbenzenesulfonate | HCID 13961807 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | S-Tetrahydro-2H-pyran-4-YL ethanethioate | HCID 18533108 | 81.3% |
Reaction Steps
To a solution of 300 g (1.175 mol) of toluene-4-sulfonic acid tetrahydropyran-4-yl ester in DMF (3 L) are added 268 g (2.35 mol) potassium thioacetate, followed by a catalytic amount of NaI (0.12 g, 10 mol %) at room temperature. After complete addition, the reaction is heated to 50° C. for 20 h. The reaction mixture is partitioned between TBME (3 L) and water (3 L), the aqueous layer is extracted with TBME (2 L), then saturated with NaCl and extracted again with TBME (2×2 L). The combined organic extracts are dried over Na2SO4, filtered and the solvent is removed under reduced pressure to afford 153 g of thioacetic acid S-(tetrahydro-pyran-4-yl)ester. Yield: 81%; ES-MS: m/z 161 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372874B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-8d1f75d8a7c44ba88b203fe57d0003a6 |
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| Source note | uspto-grants-2013_02 |
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