HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(4-iodobenzyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Iodobenzylamine | HCID 2737533 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(4-iodobenzyl)acetamide | HCID 23111624 | — |
Reaction Steps
4-Iodobenzylamine (5.32 g) was dissolved in chloroform (50 ml), and, under ice-cooling, pyridine (2.76 ml) and acetic anhydride (2.58 ml) were added and the mixture was stirred for 4 hr. The reaction mixture was washed successively with water, 1N-hydrochloric acid, water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:2-1:3) to give the title compound (5.18 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285572B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-d51619f0bc904781bb7f3e4df4788d03 |
| Source note | uspto-grants-2007_10 |