HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrazole → Methyl (5-tert-butyl-1H-pyrazol-3-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Amino-5-tert-butylpyrazole | HCID 522787 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl (5-tert-butyl-1H-pyrazol-3-yl)carbamate | HCID 13469501 | 26.8% |
Reaction Steps
10 g of 3-amino-5-t-butylpyrazole as prepared in Reference Example (this pyrazole compound being hereinafter referred to as "Compound [II]") was dissolved in 100 ml of carbon tetrachloride, and 6.8 g of methyl chloroformate was added to the solution. The mixture was then allowed to react for 5 hours under refluxing. After cooling the reaction solution, a potassium carbonate aqueous solution was added thereto whereby crystals were formed. The crystals were collected by filtration, and washed with carbon tetrachloride and water to obtain 3.8 g of methyl N-(5-t-butyl-3-pyrazolyl)carbamate. This compound was recrystallized from a mixed solvent of carbon tetrachloride and chloroform and found to have a melting point of 177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04501606 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-e91c6fe96a9642a5a48384cf49a8d376 |
| Source note | uspto-grants-1985_02 |