Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 86748808 | HCID 86748808 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19919985 | HCID 19919985 | — |
Reaction Steps
0.41 g of m-chloroperbenzoic acid was added little by little to a solution of 0.75 g of N-[2-(3-chloro-5-trifluoromethyl-2-pyridylthiomethyl)phenyl]carbamate obtained in the same manner as Synthesis Example 1 (Compound No. 1) in 20 ml of methylene chloride under stirring At room temperature. After completion of the addition, the reaction was continued at room temperature for 20 hours. The reaction mixture was poured into water, subjected to extraction with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The resulting residue was washed with hexane. The precipitated solid was filtered off to obtain 0.66 g of the desired product (Compound No. 60) having a melting point of 160° to 162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05436267 |
|---|
| Source dataset | uspto-grants-1995_07 |
|---|
| ORD ID | ord-5190347feb5c4dd6a3866ad2a2fc4fb0 |
|---|
| Source note | uspto-grants-1995_07 |
|---|