HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-[(Butylthio)methylene]-6-ethylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | HCID 70624727 | HCID 70624727 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[(Butylthio)methylene]-6-ethylcyclohexanone | HCID 53766308 | — |
Reaction Steps
A solution of 2-ethyl-6-(hydroxymethylene)cyclohexanone (43.0 g, 0.277 mole), described in Example 2, butylmercaptan (28.6 g, 0.318 mole) and p-toluenesulfonic acid (50 mg) in dry benzene (200 ml) is heated at reflux under nitrogen for 4 hr using a Dean-Stark water separator. The reaction mixture is cooled and washed with saturated aqueous sodium bicarbonate (50 ml), water and brine, then dried (MgSO4). After removal of the solvent at reduced pressure the residue is distilled to give the title compound, bp 110° - 115° C/1.5 mm, nmr (CDCl3) δ 0.92 (6H), 7.5 (m,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04057559 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-4b10890d253445b8ac7b2d134399e91f |
| Source note | uspto-grants-1977_11 |