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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538626Generated: October 31, 2026

Tetrahydro-2H-pyran-4-yl 4-methylbenzenesulfonate → S-Tetrahydro-2H-pyran-4-YL ethanethioate

https://huagongshe.com/reaction/538626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydro-2H-pyran-4-yl 4-methylbenzenesulfonateHCID 13961807—
ReactantPotassium ethanethioateHCID 23670855—
CatalystSodium IodideHCID 5238—
SolventDimethylformamideHCID 6228—
ProductS-Tetrahydro-2H-pyran-4-YL ethanethioateHCID 1853310881.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 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 RT. 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 aq. 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%; ESI-MS: 161 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865744B1
Source datasetuspto-grants-2014_10
ORD IDord-b6c0326b5db24e7cb87ed512d00feaf8
Source noteuspto-grants-2014_10