HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloromethanesulfenyl chloride → HCID 13093902, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloromethanesulfenyl chloride | HCID 11666 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13014425 | HCID 13014425 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13093902 | HCID 13093902 | — |
Reaction Steps
To 290 mg of NaOH in 15 ml of water, cooled in an ice bath, is added 1.0 g (3.56 mol) of 5-cyano-1-(4-trifluoromethylphenyl)uracil. Then 15 ml of dichloromethane is added, followed by 0.725 ml of trichloromethanesulphenyl chloride in 1.5 ml of dichloromethane. The mixture is stirred for approximately 2 hours at 5°. Then dichloromethane and ice cold water are added and the layers separated. The organic phase is washed with ice cold water, dried over MgSO4 and evaporated. The product is taken up with ether, filtered and washed again with ether to yield 5-cyano-3-trichloromethanesulphenyl-1-(4-trifluoromethylphenyl)uracil, m.p. 167°-168.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307098 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-e394cdac01ca466ca6d1462ef83cebab |
| Source note | uspto-grants-1981_12 |