HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-(3-Bromophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Product | N-(3-Bromophenyl)acetamide | HCID 12123 | — |
Reaction Steps
A solution of 3-bromo-phenylamine (1.04 g, 6 mmol) was treated with DIEA (2.3 mL, 13.3 mmol) and chilled to zero degrees. Acetyl chloride (0.47 mL, 6.7 mmol) was added dropwise via syringe. Reaction was allowed to return to room temperature and stir for 1 hour. Reaction was then poured onto water and washed once. Organic phase was evaporated to beige solids (1.25 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138199B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-02fd3887b81541678152155f58efb867 |
| Source note | uspto-grants-2012_03 |