HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-[[Acetyl[4-(tetradecyloxy)benzoyl]amino]methyl]-1-(phenylmethyl)pyridinium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | N-Acetyl-N-(2-pyridinylmethyl)-4-(tetradecyloxy)benzamide | HCID 11754296 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[[Acetyl[4-(tetradecyloxy)benzoyl]amino]methyl]-1-(phenylmethyl)pyridinium bromide | HCID 10461765 | 50.2% |
Reaction Steps
A mixture of 0.75 g of product from Example 5, 0.412 g of benzyl bromide and 3 ml of acetonitrile is stirred at room temperature for 17.5 hours then heated, in a sealed tube, at 100° C. for 21.25 hours. The cooled reaction mixture is concentrated in vacuo and the residue purified by column chromatography (silica gel: 10% methyl alcohol/chloroform) to give 0.515 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05208247 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-278fac69d2954beea6dae9c36d44ea40 |
| Source note | uspto-grants-1993_05 |