HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → HCID 178505109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 178503861 | HCID 178503861 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178505109 | HCID 178505109 | — |
Reaction Steps
The N-methylsulphonyl-N'-(3,4-dichlorophenyl)-S-methylisothiourea (150 g) obtained in the manner described was suspended in 250 ml of ethyl acetate, and 45 ml of sulphonyl chloride (0.55 mole) was added dropwise to the suspension at a temperature of 50° C. The solvent as well as the formed methanesulphonyl chloride and unreacted sulphonyl chloride was distilled off in the Rotovap, and the crystallising residue was taken up in hexane. After filtration with suction, the resulting N-methylsulphonyl-N'-(3,4-dichlorophenyl)-chloroformamidine had a melting oint of 154° - 156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04098900 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-420550699bc145b496896461e5df73b0 |
| Source note | uspto-grants-1978_07 |