HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2-Bromo-N-Methylsulfonylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-N-Methylsulfonylacetamide | HCID 262944 | — |
Reaction Steps
Sodium hydride (1.68 g×60% ) was added to a stirred solution of methanesulfonamide (2.0 g) in dry tetrahydrofuran (20 ml) at room temperature. The resulting solution was stirred at room temperature for 1 hour, as which time it was treated with a solution of bromoacetyl bromide (4.2 g) in dry tetrahydrofuran (10 ml). After 1 hour the solvent was removed under reduced pressure and the residue taken up in water and acidified to pH3. The acidic solution was extracted into ethyl acetate, dried (MgSO4), filtered and the solvent removed under reduced pressure. Recrystallisation from isopropanol afforded the product as white needles: mp 112°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620989 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-575b933edd854cfcb80aab968d02232c |
| Source note | uspto-grants-1997_04 |