HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754042Generated: October 28, 2026
Methane → 2-(Acetyloxy)-4-(methylsulfanyl)butanoic acid
https://huagongshe.com/reaction/1754042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | alpha-Hydroxy-gamma-methylmercaptobutyric acid | HCID 11427 | — |
| Product | 2-(Acetyloxy)-4-(methylsulfanyl)butanoic acid | HCID 3074728 | 63.1% |
Reaction Steps
To a solution of 2-hydroxy-4-(methylthio)butanoic acid (50.74 g, 337.8 mmol, obtained by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap) in dichloromethane (1 L) was added triethylamine (93 mL, 667.3 mmol) and the resulting mixture was cooled to 0° C. To the cooled mixture was added acetyl chloride (26 mL, 365.6 mmol) dropwise. The ice bath was removed and the reaction was allowed to warm to room temperature overnight. The reaction was washed with 1N HCl (2×300 mL), and brine (1×300 mL), dried over magnesium sulfate, filtered and evaporated to give an amber oil (59.82 g, 63.1%). m/z 193 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169203B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8a45b48979be4167b65dfe0a1edf247a |
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| Source note | uspto-grants-2015_10 |
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