HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzenesulfonyl chloride → HCID 67863379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 15670382 | HCID 15670382 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67863379 | HCID 67863379 | 96.6% |
Reaction Steps
To a suspension of (2S,4R)-4-(4-chlorophenyl-sulfonylamino)-2-[(Z)-2-(4-methoxycarbonylphenyl)vinyl]pyrrolidine (11.5 g) in dichloromethane (200 ml) were added triethylamine (3.80 ml) and 4-chlorobenzenesulfonyl chloride (5.77 g) under ice bath cooling and the mixture was stirred at room temperature for 1 hour. The solution was washed successively with diluted hydrochloric acid, saturated aqueous sodium bicarbonate and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residual solid was collected by filtration to give (2S,4R)-1-(4-chlorophenylsulfonyl)-4-(4-chlorophenylsulfonylamino)-2-[(Z)-2-(4-methoxycarbonylphenyl)vinyl]pyrrolidine (15.71 g) as a white powder
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916152 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-7341c31f5ac1463caa535987df47aaa8 |
| Source note | uspto-grants-1990_04 |