Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl vinyl sulfone | HCID 19354 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13502056 | HCID 13502056 | 38.7% |
Reaction Steps
To a stirred solution of 53.2 g (0.5 mole) methylvinylsulfone and 1 ml triethylamine in 50 ml methanol, 38.06 g [35.75 ml (0.5 mole)] thioacetic acid was added dropwise over 15 minutes. During the addition, the temperature was maintained between 30°-40° C. with an ice bath. The mixture was stirred overnight at room temperature; then the solvent was removed using a rotovap to give a yellow-red oil which solidified upon cooling. The residue was dissolved in 150 ml of hot ethyl acetate; then 100 ml hexane was added. With cooling of the solution in an ice bath, fine white needle crystals formed. The crystals were recovered by filtration, were washed with cold 1:1 ethyl acetate:hexane and air-dried to give 35.28 g of the above-identified product as a crystalline solid, melting point 57°-59° C. A second crop of 29.13 g crystals melting point 57°-60° C. was obtained to give a total of 64.41 g of the above-identified product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04652556 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-5e252b5f8a564454924299e558dd54f0 |
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| Source note | uspto-grants-1987_03 |
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