HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 5-t-butyl-2-methoxy-3-(chloroacetamido) phenyl N-t-butylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-t-butyl-2-methoxy-3-aminophenyl N-t-butyl sulfonamide | HCID 15029586 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-t-butyl-2-methoxy-3-(chloroacetamido) phenyl N-t-butylsulfonamide | HCID 15029587 | — |
Reaction Steps
A solution of chloroacetyl chloride (4.4 ml) in dichloromethane (40 ml) was added dropwise to a cooled and stirred solution of 5-t-butyl-2-methoxy-3-aminophenyl N-t-butyl-sulfonamide (15.6 g) and diisopropylethylamine (9.5 ml) in dichloromethane (100 ml). The solution was left standing at ambient temperature for 2 hours and then washed with a 2% solution of citric acid. The organic phase was dried and evaporated. Recrytallization from aqueous ethanol gave the title compound (16.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929269 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-979e8240d54b4415a395bd82d5be5d51 |
| Source note | uspto-grants-1990_05 |