HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N-(tert-Butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide | HCID 68288463 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide | HCID 68287917 | — |
Reaction Steps
A solution of 0.66 g of N-(tert-butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide, 1.85 g of ammonium acetate and 0.17 g of sodium cyanoborohydride in 12 ml of methanol was stirred at 60° C. for 17 hours. After the removal of the solvent under reduced pressure, the residue was taken up in 50 ml of ethyl acetate and washed twice with 30 ml of 0.5 N aqueous sodium hydroxide solution and 30 ml of saturated aqueous sodium chloride solution. The organic phase was dried over MgSO4 and concentrated by rotary evaporation. The crude product was subjected to a chiral separation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08828994B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-862b77b448334435a0c2e674fe13fedc |
| Source note | uspto-grants-2014_09 |