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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

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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372874B2
Source datasetuspto-grants-2013_02
ORD IDord-8d1f75d8a7c44ba88b203fe57d0003a6
Source noteuspto-grants-2013_02