HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-(Acetylaminomethyl)-6-bromoacetylpyridine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Acetyl-6-(acetylaminomethyl)pyridine | HCID 10375315 | — |
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Acetylaminomethyl)-6-bromoacetylpyridine hydrobromide | HCID 18953871 | — |
Reaction Steps
A solution of bromine (1.56 g) in acetic acid (5 ml) was added dropwise to a solution of 2-acetyl-6-(acetylaminomethyl)pyridine (1.87 g) and 30 weight % hydrogen bromide-acetic acid solution (4.2 ml) in a mixture of acetic acid (40 ml) and methanol (10 ml) at ambient temperature with stirring. The mixture was warmed to 60° to 70° C. and stirred for two hours. The solvent was evaporated in vacuo and the residue was triturated with diisopropyl ether to give 2-(acetylaminomethyl)-6-bromoacetylpyridine hydrobromide (3.78 g). IR (Nujol) : 1720, 1620 cm-1 NMR (CD3OD, δ): 2.10 (3H, s), 3.90 (2H, s), 4.83 (2H, s), 7.77 (1H, br s), 8.13 (2H, t, J=8 Hz) and 8.70 (1H, t, J=8 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371097 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-68195fd4f4704a72b489969f8b56c116 |
| Source note | uspto-grants-1994_12 |