HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Benzenamine, 4-butyl-2-nitro- | HCID 77229 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide | HCID 21482995 | 86.8% |
Reaction Steps
A solution of 4-n-butyl-2-nitroaniline (29.1 g) in toluene (100 ml) was treated with bromoacetyl bromide (33.3 g). The mixture was boiled under reflux for 3/4 hour and the toluene evaporated off. The residual oil was poured into petroleum spirit (b.p. 60°-80° C; 400 ml). Crystals were deposited and these were removed by filtration to give N-(4-n-butyl-2-nitrophenyl)-2-bromoacetamide (41 g), m.p. 56°-57° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005217 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-34f540d0d41d41dbb854a8055330ba82 |
| Source note | uspto-grants-1977_01 |