HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfur dichloride → 3,4-Dichlorophenylmethanesulfenyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfur dichloride | HCID 25353 | — |
| Reactant | 3,4-Dichlorotoluene-alpha-thiol | HCID 118986 | — |
| Reactant | HCID 178526253 | HCID 178526253 | — |
| Product | 3,4-Dichlorophenylmethanesulfenyl chloride | HCID 21409968 | — |
Reaction Steps
3,4-Dichlorophenylmethanesulfenyl chloride is prepared from the corresponding 3,4-dichlorobenzyl mercaptan in accordance with the procedure of Example I for the preparation of the sulfenyl chloride, except that this reaction is conducted under cooling conditions. The sulfenyl chloride is reacted with the mercaptopyridine-1-oxide as described in Example I, giving an 84% yield of 3,4-dichlorobenzyl 1-oxo-2-pyridyl disulfide having a melting point of 133.0°-134.0° C. and
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049665 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-69bfa39ad1c94840afdd79f2dfbe0599 |
| Source note | uspto-grants-1977_09 |