HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → HCID 21497805, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(4-Acetamidophenoxy)-3-amino-5-sulfamoylbenzoic acid | HCID 21497838 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21497805 | HCID 21497805 | — |
Reaction Steps
The starting material is prepared as follows: To the mixture of 3.6 g of 4-(4-acetamidophenoxy)-3-amino-5-sulfamoylbenzoic acid, 10 ml of water and the sufficient amount of N aqueous sodium hydroxide to reach a pH = 7.4, 1.3 g of benzyl chloride are added while stirring at 30°. The mixture is stirred for 16 hours at room temperature, during which time 4N aqueous sodium hydroxide is added dropwise to keep said pH value. It is filtered, the filtrate acidified with glacial acetic acid and the precipitate formed filtered off, to yield the 4-(4-acetamidophenoxy)-3-benzylamino-5-sulfamoylbenzoic acid which, on recrystallization from aqueous ethanol, melts at 255° with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03982018 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-d519f5143dc444e8a0893f9ffa34daef |
| Source note | uspto-grants-1976_09 |