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Pyrazole → Methyl (5-tert-butyl-1H-pyrazol-3-yl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyrazole | HCID 1048 | — |
| 反応物 | Methyl chloroformate | HCID 6586 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-Amino-5-tert-butylpyrazole | HCID 522787 | — |
| 溶媒 | Carbon Tetrachloride | HCID 5943 | — |
| 生成物 | Methyl (5-tert-butyl-1H-pyrazol-3-yl)carbamate | HCID 13469501 | 26.8% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04501606 |
| 出典データセット | uspto-grants-1985_02 |
| ORD ID | ord-e91c6fe96a9642a5a48384cf49a8d376 |
| 出典メモ | uspto-grants-1985_02 |