HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-ethoxycarbonyl-N'-chlorothiocarbonylhexahydropyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 1(2H)-Pyridazinecarboxylic acid, tetrahydro-, ethyl ester | HCID 3014377 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-ethoxycarbonyl-N'-chlorothiocarbonylhexahydropyridazine | HCID 53642385 | — |
Reaction Steps
With the temperature maintained at 30° or below, a mixture of N-ethoxycarbonylhexahydropyridazine (1.5 g, 9.49 mmol) and triethylamine (1.0 g, 9.49 mmol) in 8 ml of benzene is added dropwise to a stirring solution of thiophosgene (1.1 g, 9.49 mmol) in 10 ml of benzene. The reaction is stirred at RT for 4 hours, and is then diluted with benzene to 50 ml, quickly washed with water and with brine, dried and stripped to give N-ethoxycarbonyl-N'-chlorothiocarbonylhexahydropyridazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04406689 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-0454f0475099429ca02a5bac0249db6a |
| Source note | uspto-grants-1983_09 |