Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231402Generated: October 31, 2026

Methanol → HCID 86742519, compound

https://huagongshe.com/reaction/2231402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Acetoxy-3-methylthiopropeneHCID 54439354—
ReactantHCID 86132149HCID 86132149—
ReactantHCID 178418416HCID 178418416—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
ProductHCID 86742519HCID 8674251910%

Reaction Conditions

Temperature120 °C

Reaction Steps

0.5 mmoles 1-acetoxy-3-methylthiopropene, (Z:E ratio 43:57), and 2.5 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 CH3CN 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 500 psi (at room temperature) was charged to the bomb, and the bomb was heated to 120° 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 3 percent, and that 2-acetoxy-4-(methylthio)thiobutanoic acid, methyl ester was produced in a yield of 10 percent, based on the 1-acetoxy-3-methylthiopropene reactant charged. 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-37562bec23b04a829bf29e735c6473a4
Source noteuspto-grants-1988_11