HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754034Generated: October 24, 2026
Methane → Butanoic acid, 2-hydroxy-4-(methylthio)-, hexyl ester
https://huagongshe.com/en/reaction/1754034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 1-Hexanol | HCID 8103 | — |
| Reactant | alpha-Hydroxy-gamma-methylmercaptobutyric acid | HCID 11427 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Butanoic acid, 2-hydroxy-4-(methylthio)-, hexyl ester | HCID 10014278 | — |
Reaction Steps
To a 4 neck 1 L round bottom flask fitted with a reflux condenser, dean stark trap, thermocouple, and mechanical overhead stirrer was added 2-hydroxy-4-(methylthio)butanoic acid (100 g, 666 mmol, obtained for example by stirring Alimet over activated charcoal, filtering and concentrating in a rotovap), 1-hexanol (125.4 mL, 999 mmol), sodium hydrogen sulfate (1.60 g, 13.32 mmol), and toluene (500 mL). The reaction was heated to reflux with removal of water (20 mL) during the course of about 5.5 hours and the reaction was monitored by GC analysis. The reaction was cooled to room temperature overnight and the organic layer was washed with saturated NaHCO3 (1×250 mL), DI water (1×250 mL) and brine (2×250 mL), dried over sodium sulfate, filtered and evaporated to give a brown oil (253.3 g). The oil was purified by kugelrohr distillation at 100° C. and 0.1 Torr vacuum to give a colorless oil (100.0 g, 64.1%). m/z 257 (MNa+).
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-1aa00c471ae14729b3732a9de8bc8fbe |
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| Source note | uspto-grants-2015_10 |
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