HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzenesulfenylchloride → HCID 131712906, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzenesulfenylchloride | HCID 11084465 | — |
| Reactant | HCID 13066428 | HCID 13066428 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131712906 | HCID 131712906 | — |
Reaction Steps
2-Thiocyanomethylthio-4,4-dimethyl-5-methylenethiazoline, 4.0 gm (prepared in a manner consistent with Examples 1 and 2) was added to 100 ml of dichloromethane. 3.11 gm of 4-chlorophenylthiochloride was added to the system. The system was stirred at room temperature for 48 hours. The product precipitated from solution. The product was filtered and air-dried to give 4.7 gm of the 2-thiocyanomethylthio-4,4-dimethyl-5-(4-chlorophenylthio)methylenethiazoline as an off-white solid, m.p. 122°-131° C. Listed as compound number 1 in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04365989 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-ea97bc8d012d4b56a8d73340f5db1075 |
| Source note | uspto-grants-1982_12 |