HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Allyl(4-methylphenyl) sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Silane, trimethyl[(4-methylphenyl)thio]- | HCID 11095572 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Allyl(4-methylphenyl) sulfide | HCID 232029 | 85% |
Reaction Steps
5.1 ml (59 mmoles) of allyl bromide were added to a mixture of 10.04 g (51.2 mmoles) of p-tolylthio(trimethyl)silane in 20 ml of acetonitrile and 18 ml of hexamethylphosphoric triamide and the conversion was complete after stirring for 20 minutes at room temperature. The reaction mixture was treated as described in Example 3 to obtain 7.1 g (85% yield) of allyl p-tolyl sulfide boiling at 110°-111° C./14 mm Hg and having a refractive index of nD25 =1.5644.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496720 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-0983db5433f64ec28272cbfab33d2e66 |
| Source note | uspto-grants-1985_01 |