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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | 5-(Methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 152111 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[(Ethylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 13505759 | 60.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04547516 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-e6587b2be0d14518b4018413b16f9be2 |
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| Source note | uspto-grants-1985_10 |
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