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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231397Generated: October 31, 2026

Methanol → HCID 86742519, compound

https://huagongshe.com/reaction/2231397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Acetoxy-3-methylthiopropeneHCID 54439354—
ReactantHCID 86132149HCID 86132149—
ReactantHCID 178418416HCID 178418416—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86742519HCID 8674251916.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

0.5 mmoles 1-acetoxy-3-methylthiopropene, (Z: E ratio 43:5.7), and 10 mmoles methanol were charged into a 71 cc stainless steel bomb equipped with a glass liner and a Teflon coated.stir bar. Ten mole percent, based on 1-acetoxy-3-methylthiopropene, of a catalyst comprising bis(triphenylphosphine)dichloropalladium, (φ3P)2PdCl2, was added. Toluene was included as an internal standard. Five milliliters of tetrahydrofuran as a solvent were also included in the reaction system. The reaction mixture was charged under argon. The bomb was sealed and carbon monoxide at a pressure of 1000 psi (at room temperature) was charged to the bomb, and the bomb was heated to 100° C. and allowed to react for 44 hours with stirring. At the termination of the reaction, the reaction products were analyzed by gas chromatography and it was found that 2-acetoxy-4-(methylthio)butanoic acid, methyl ester was produced in a yield of 28.6 percent, and that 2-acetoxy-4-(methylthio)thiobutanoic acid, methyl ester was produced in a yield of 16.8 percent, based on the 1-acetoxy-3-methylth.1opropene reactant charged. Note that each of the products is hydrolyzable to methionine hydroxy analog.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782173
Source datasetuspto-grants-1988_11
ORD IDord-906c313b99bd4745ac50a9b2895a239a
Source noteuspto-grants-1988_11