HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → O-(1-isopropylpyrazol-4-yl) N-(2-cyanoprop-2-ylsulphenyl)-N-methyl-carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Propan-2-yl)-1H-pyrazol-4-ol | HCID 13018411 | — |
| Reactant | N-(2-cyanoprop-2-ylsulphenyl)-N-methyl-carbamoyl fluoride | HCID 13340646 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | O-(1-isopropylpyrazol-4-yl) N-(2-cyanoprop-2-ylsulphenyl)-N-methyl-carbamate | HCID 13340647 | 85% |
Reaction Steps
12 g (0.075 mole) of N-(2-cyanoprop-2-ylsulphenyl)-N-methyl-carbamoyl fluoride are added dropwise to a mixture of 9.45 g (0.075 mole) of 4-hydroxy-1-isopropylpyrazole, 8.5 g (0.085 mole) of triethylamine and 100 ml of toluene at 25° C. When the addition has ended, the mixture is stirred at room temperature for 18 hours. For working up, the reaction mixture is washed twice with water, dried over sodium sulphate and freed from the solvent in vacuo. 18 g (85% of theory) of O-(1-isopropylpyrazol-4-yl) N-(2-cyanoprop-2-ylsulphenyl)-N-methyl-carbamate are obtained in the form of a yellow oil of refractive index nD21 1.5070.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04535091 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-adac67ad5f4b4ce38650cf05607271b5 |
| Source note | uspto-grants-1985_08 |