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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628770Generated: November 1, 2026

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

https://huagongshe.com/reaction/628770

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 tetrahydro-pyran-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]; 1H-NMR (250 MHz, CHLOROFORM-d) δ ppm 1.47-1.98 (4 H, m), 2.30 (3 H, s), 3.41-3.74 (3 H, m), 3.88 (2 H, dt, J=11.76, 3.86 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315454B2
Source datasetuspto-grants-2016_04
ORD IDord-62c0de0ff38c4677afb6738f950145d4
Source noteuspto-grants-2016_04