HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → N-(4-bromo-2-nitrophenyl)-2-chloroacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | 4-Bromo-2-nitroaniline | HCID 70132 | — |
| Product | N-(4-bromo-2-nitrophenyl)-2-chloroacetamide | HCID 16457083 | 96% |
Reaction Steps
To a solution of 4-bromo-2-nitroaniline (15.0 g, 69.1 mmol) was added drop wise 2-chloroacetyl chloride (9.4 g, 82.9 mmol) under nitrogen. After refluxing for 1.5 h, the reaction mixture was cooled to ambient temperature and the solvent was removed under reduced pressure. Crystallization from ethyl acetate/hexane afforded N-(4-bromo-2-nitrophenyl)-2-chloroacetamide (19.4 g, 66.1 mmol, 96%) as yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541404B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-ffe1c224bf7a4abdb0904482ad6ae5ce |
| Source note | uspto-grants-2013_09 |