HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 13425461, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13425461 | HCID 13425461 | — |
Reaction Steps
Thiophenol, 11.0 g (0.10 mole), was added dropwise over a period of one hour, to a cold (0° C.) mixture of 13.69 g [8.5 ml (0.1 mole)] 1-bromo-2,3-epoxypropane (epibromohydrin), 1.5 ml [1.09 g (0.02 moles)] triethylamine and 1.5 ml methanol. The reaction mixture was then allowed to come to room temperature and was stirred at room temperature overnight. The solvent was removed in vacuo. The residue was dissolved in ether, washed several times with water and once with brine. The organic phase was dried over magnesium sulfate, filtered and concentrated to give 22.7 g of the above-identified product as an amber oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04602030 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-b78660d3255b4646909b5fbb26c1d9b9 |
| Source note | uspto-grants-1986_07 |