HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzenesulfonyl chloride → Methyl [2-[(4-chlorophenyl)sulfonylamino]indan-5-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | dibenzoyl-L(+)tartaric acid | HCID 12362976 | — |
| Reactant | Methyl (-)-(2-aminoindan-5-yl)acetate | HCID 14071505 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl [2-[(4-chlorophenyl)sulfonylamino]indan-5-yl]acetate | HCID 53769737 | — |
Reaction Steps
Methyl (-)-(2-aminoindan-5-yl)acetate.(-)-dibenzoyl-L-tartaric acid salt (3.94 g) is added to a mixture of potassium carbonate (4.83 g), water (50 ml) and ethyl acetate (70 ml), and 4-chlorophenylsulfonyl chloride (1.49 g) is added thereto. The mixture is stirred at room temperature for one hour. The ethyl acetate layer is separated from the reaction mixture, washed with an aqueous sodium hydrogen carbonate solution, dried, and distilled under reduced pressure to remove the solvent. The residue is recrystallized from a mixture of ethyl acetate and hexane to give methyl (-)-[2-[(4-chlorophenyl)sulfonylamino]indan-5-yl]acetate (2.43 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05030652 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-531c47868786454ab6d07d77d8c9fd47 |
| Source note | uspto-grants-1991_07 |