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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464406Generated: October 27, 2026

Ethanethiol → 5-[(Ethylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione

https://huagongshe.com/reaction/464406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
Reactant5-(Methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 152111—
SolventEthanolHCID 702—
Product5-[(Ethylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 1350575960.8%

Reaction Steps

5-(Methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (7 g, 38 mmole), described by Bihlmayer et al., supra, was suspended in ethanol (70 ml). The suspension was stirred vigorously while being subjected to the addition of ethanethiol (12.85 g, 200 mmole). The mixture was heated at reflux until all the starting material had been consumed, as indicated by thin layer chromatography (silica gel plates, 30% ethyl acetate in hexane). The volatile portion of the reaction mixture was removed by distillation under reduced pressure. The residue was purified by high pressure liquid chromatography (HPLC, 20% ethyl acetate in hexane, v/v). The purest fractions were combined. The solvent was removed under reduced pressure. The residue was crystallized to give 5.0 g of the title compound; mp 52°-54° C.; NMR (CDCl3) δ 1.45 (t, 3H), 1.7 (s, 6H), 3.02 (q, 2H), 9.0 (s, 1H); IR (CHCl3) 1720, 1700 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547516
Source datasetuspto-grants-1985_10
ORD IDord-e6587b2be0d14518b4018413b16f9be2
Source noteuspto-grants-1985_10