HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → 2-Phenylethyl-ethyl-disulphide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | 2-Phenylethanethiol | HCID 78126 | — |
| Reactant | N-ethylthiophthalimide | HCID 57251189 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Phenylethyl-ethyl-disulphide | HCID 20306436 | 111.3% |
Reaction Steps
8 g (0.058 mol) of phenethylmercaptan are added with intensive stirring to a suspension of 12 g (0.058 mol) of N-ethylthiophthalimide in 70 ml of benzene. After a few minutes, a homogeneous solution forms and the phthalimide slowly begins to precipitate out therefrom. After stirring for 48 hours at room temperature, the mixture is filtered through a paper filter, the filtrate is concentrated in a vacuum and the crude 2-phenylethyl-ethyl-disulphide (12.8 g) obtained is distilled through a Vigreux column. There are thus obtained 10.5 g of pure product (91% of theory) which has a purity of 99% (gas-chromatographic estimation). Boiling point 87-88 mm Hg/0.04 mm Hg; nD20 =1.5742.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04170594 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-05445a39f4be4c6e8130d9856d7d6cd7 |
| Source note | uspto-grants-1979_10 |