HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → Trans-4-(2-acetylamino-cyclopentyl)-benzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | N-(2-Phenyl-cyclopentyl)-acetamide | HCID 66645957 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Trans-4-(2-acetylamino-cyclopentyl)-benzenesulfonyl chloride | HCID 58433496 | — |
Reaction Steps
4.7 g of the crude product of example 2a were dissolved in 90 ml of dichloromethane. To this mixture 5.4 ml of chloro sulfonic acid were added drop by drop under stirring at room temperature. The reaction mixture was heated at 50° C. for 1 hour and, after cooling to room temperature, triturated with 70 ml of ice water. After separating the organic layer was dried over sodium sulfate and evaporated to dryness yielding 4.4 g of the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344004B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-dbdb4243f3164315bae13e61b12e70f7 |
| Source note | uspto-grants-2013_01 |