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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307481Generated: October 25, 2026

Water → 4a'-methyl-(4'H,5'H,7'H)-spiro[1,3-dithiolane-2,2'-naphthalen]-5'(6'H)-one

https://huagongshe.com/reaction/2307481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,2-EthanedithiolHCID 10902—
Reactant(+-)-Wieland-Miescher ketoneHCID 89262—
SolventAcetic AcidHCID 176—
Product4a'-methyl-(4'H,5'H,7'H)-spiro[1,3-dithiolane-2,2'-naphthalen]-5'(6'H)-oneHCID 8730635287.3%

Reaction Steps

To a solution of Wieland-Miescher ketone (5.87 g, 33.0 mmol) in glacial acetic acid (40 mL) was added p-toluenesulfonic acid (2.94 g) followed by dropwise addition of 1,2-ethanedithiol over a 1 hour period. The reaction mixture was stirred at room temperature for another 4 hours, poured into 30 mL water, and stirred for 15 minutes. The white solid was filtered off, washed successively with water, diluted with NaHCO3 solution and water, and then dried to yield thioketal 239 (7.33 g, 87.3 %) as a white solid. 1H NMR (CDCl3) δ 1.50-2.70 (m, 10H), 3.20-3.40 (m, 4H), 5.67 (s, 1H); 13C NMR (CDCl3) 212.92, 141.23, 128.04, 64.81, 49.43, 40.11, 39.62, 37.92, 37.57, 30.81, 30.69, 24.73, 24.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831093B2
Source datasetuspto-grants-2004_12
ORD IDord-e50d7a69aa864268b1821b4e2fb770ee
Source noteuspto-grants-2004_12