HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → 1-(benzenesulfonyl)-octahydro-1H-indole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Octahydroindole-2-carboxylic acid | HCID 3274680 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(benzenesulfonyl)-octahydro-1H-indole-2-carboxylic acid | HCID 21714126 | — |
Reaction Steps
29.8 mmol (3.8 ml) of benzenesulphonyl chloride and 7.4 ml of 4M sodium hydroxide solution are added in succession to a solution, cooled to 0° C., of 29.6 mmol (5 g) of 2-perhydroindolecarboxylic acid in 7.4 ml of 4M NaOH. The reaction mixture is left at room temperature, with stirring, for 24 hours. The mixture is then rendered acidic to pH 2-3 and filtered. The resulting solid is washed with ether to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271247B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-f669244576054fe181f75fff73fd0550 |
| Source note | uspto-grants-2001_08 |