HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 21520060, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21520079 | HCID 21520079 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21520060 | HCID 21520060 | — |
Reaction Steps
3-Mercapto-4-phenoxy-5-sulfamylbenzoic acid (0.6 g) is suspended in water (20 ml) and the pH is adjusted to 8 by addition of 1 N sodium hydroxide. Benzyl bromide (0.35 g) is added to the resulting solution, and the reaction mixture is stirred for 2 hours at room temperature. After cooling, the precipitated sodium salt of 3-benzylthio-4-phenoxy-5-sulfamylbenzoic acid is collected by filtration. The salt is dissolved in hot water (60 ml) and the solution acidified by addition of 1 N hydrochloric acid. After cooling, the precipitated 3-benzylthio-4-phenoxy-5-sulfamylbenzoic acid is collected by filtration and recrystallized from aqueous ethanol to yield the desired compound with a melting point of 234°-236°C., after drying in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03972886 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-3bd6afdb58f1402d8ddbd254ab2485cf |
| Source note | uspto-grants-1976_08 |