Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Acetoxy-3-methylthiopropene | HCID 54439354 | — |
| Reactant | HCID 86132149 | HCID 86132149 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86742519 | HCID 86742519 | 16.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04782173 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-906c313b99bd4745ac50a9b2895a239a |
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| Source note | uspto-grants-1988_11 |
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