HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Fluoro-4-methylphenyl methyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Fluoro-4-methylaniline | HCID 9957 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-Fluoro-4-methylphenyl methyl sulfide | HCID 53414492 | 525.5% |
Reaction Steps
A mixture of 3-fluoro-4-methylaniline (25 g), dimethyl disulphide (375 g) and t-butyl nitrite (30 ml) in 1,2-dichloroethane was warmed to start the reaction. A solution of 3-fluoro-4-methylaniline (225 g) in 1,2-dichloroethane was added dropwise, simultaneously with t-butyl nitrite (241 ml) at such a rate as to maintain the temperature below 60° C. The mixture was stirred for 2 hours, then water was added. The organic layer was washed with water, hydrochloric acid, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness and the residue was distilled to give 2-fluoro-4-(methylsulphenyl)toluene (164 g) as a yellow oil; NMR (acetone-d6); 2.2 (3H,d), 2.5 (3H,s), 7.05 (3H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424276 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-9b753ec268a24204821843de40f5cfd5 |
| Source note | uspto-grants-1995_06 |