HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069841Generated: October 30, 2026
Acetic Anhydride → 2-Acetamido-5-bromopyridine
https://huagongshe.com/reaction/2069841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Acetamido-5-bromopyridine | HCID 293097 | 80.5% |
Reaction Steps
To a stirred solution of 5-Bromo-pyridin-2-ylamine (100 mg, 0.578 mmol) in dry THF was added acetic anhydride (70.25 mg, 0.693 mmol). The reaction mixture was stirred at 20° C. for 12 hrs. THF was distilled out and to it was added ethyl acetate. The organic layer was washed with saturated NaHCO3 solution and dried over anhy sodium sulphate. Removal of the solvent afforded N-(5-Bromo-pyridin-2-yl)-acetamide (100 mg, 80%). This was carried to next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08299077B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-d092648319d4446c8b6e67ae31ae5bbc |
|---|
| Source note | uspto-grants-2012_10 |
|---|