HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2',4'-Trichloroacetophenone → HCID 12836996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2',4'-Trichloroacetophenone | HCID 20250 | — |
| Reactant | 3-Amino-1,1-dimethylthiourea | HCID 2733700 | — |
| Product | HCID 12836996 | HCID 12836996 | — |
Reaction Steps
4.16 g (0.035 mole) of 4,4-dimethyl-thiosemicarbazide and 7.82 g (0.035 mole) of 2,4-dichlorophenacyl chloride are reacted under the conditions of Example 2. After concentration, ethyl acetate is added to the residue and further concentration is employed. A yellow, needle-like solid is produced. The solid is dried under high vacuum at 65° C. Subsequently, it is recrystallized from methanol/ethyl acetate and again dried under high vacuum to produce 5-(2,4-dichlorophenyl)-N,N-dimethyl-6H-1,3,4-thiadiazin-2-amine monohydrochloride. m.p. 219°-222° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309426 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-5dc3eb7f23214de2950e95f2b23d3559 |
| Source note | uspto-grants-1982_01 |