HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 1-Methylsulfonyl-3-methoxy-prop-1-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Propene, 3-methoxy- | HCID 69392 | — |
| Reactant | Methanesulfonyl bromide | HCID 190026 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Methylsulfonyl-3-methoxy-prop-1-ene | HCID 53828862 | 83.2% |
Reaction Steps
159 g (1 mole) of methanesulfonyl bromide are slowly added dropwise, at 45° C., to a mixture of 78 g (1.07 moles) of methyl allyl ether, 7.5 g of zinc chloride and 3.3 ml of 50% strength hydrogen peroxide. After the exothermic reaction has subsided, the mixture is stirred for a further 30 minutes and is diluted with 450 ml of benzene, and 135 g (1.33 moles) of triethylamine are added at room temperature, whilst cooling. After 2 hours, the precipitate is filtered off and the solvent is distilled off. Distillation of the residue gives 125 g of 1-methylsulfonyl-3-methoxy-prop-1-ene, boiling point 114°-115° C./0.3 mm Hg. According to the NMR spectrum, the product is a mixture of cis and trans isomers in the ratio of 15:85.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168379 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-ac6f90c904bd4e409bbe1287dcfe0238 |
| Source note | uspto-grants-1979_09 |