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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant1-HexanolHCID 8103—
Reactantalpha-Hydroxy-gamma-methylmercaptobutyric acidHCID 11427—
ReactantSodium BisulfateHCID 516919—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductButanoic acid, 2-hydroxy-4-(methylthio)-, hexyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169203B2
Source datasetuspto-grants-2015_10
ORD IDord-1aa00c471ae14729b3732a9de8bc8fbe
Source noteuspto-grants-2015_10