HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379909Generated: October 30, 2026
Bromine → N-phenyl-2-(methylsulfinyl)benzamide
https://huagongshe.com/reaction/1379909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 152460 | HCID 152460 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-phenyl-2-(methylsulfinyl)benzamide | HCID 11832126 | — |
Reaction Steps
To a 1000 ml four-necked flask equipped with a stirrer, a thermometer, and a condenser, 48.6 g (0.2 mol) of N-phenyl-2-(methylthio)benzamide obtained in Example 1, 300 g of toluene, and 200 g of a 10% by weight aqueous solution of potassium bicarbonate are placed. To the above mixture in the flask, 32.0 g (0.2 mol) of bromine is added dropwise while stirring at a temperature of from 10° to 15° C. to be allowed to react with each other for about 10 minutes. After completion of the reaction, the produced white crystals are filtered and then recrystallized from a mixture of water and ethanol (1:9) to give 48.7 g of N-phenyl-2-(methylsulfinyl)benzamide (melting point: 194° to 195° C.). The yield of the product against N-phenyl-2-(methylthio)benzamide is 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05672751 |
|---|
| Source dataset | uspto-grants-1997_09 |
|---|
| ORD ID | ord-5b6480808eeb4684a63b49f6b65059f4 |
|---|
| Source note | uspto-grants-1997_09 |
|---|