HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxide → Cymiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | 2-Chloro-1,1-diethoxyethane | HCID 12128 | — |
| Reactant | 1-(2,4-Dimethylphenyl)-3-methylthiourea | HCID 3034214 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Cymiazole | HCID 43714 | — |
Reaction Steps
19.4 g (0.1 mole) of N-2,4-xylyl-N'-methyl-thiourea and 15.2 g (0.1 mole) of chloroacetaldehyde-diethylacetal in 150 ml of 2N aqueous hydrochloric acid are refluxed for 1 hour. The clear light-yellow solution is subsequently cooled to room temperature; it is rendered slightly alkaline with 30% aqueous medium hydroxide solution, and extracted with ether. The ether extract is washed with water, dried with sodium sulphate and filtered, and the ether is then distilled off. The oily residue is distilled; b.p. 132°-134° C/0.3 Torr; yield: 20.2 g = 92% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04079144 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-17326f4df40341ea967ed5534a26a618 |
| Source note | uspto-grants-1978_03 |