HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-{[3-(Benzyloxy)pyridin-2-yl]methyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12074949 | HCID 12074949 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{[3-(Benzyloxy)pyridin-2-yl]methyl}acetamide | HCID 13217542 | — |
Reaction Steps
Add dropwise with stirring a solution of 3.5 ml acetyl chloride in 50 ml THF (tetrahydrofuran) to a cooled solution of 10 gm of 2-aminomethyl-3-phenylmethoxypyridine and 7.1 ml triethylamine in 125 ml THF. Warm to room temperature and stir an additional hour. Remove triethylamine hydrochloride by filtration and evaporate the filtrate under reduced pressure. Recrystallize the residue from toluene to obtain 2-acetamidomethyl-3-(phenylmethoxy)pyridine, mp 94°-96°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04409226 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-4d62df5a6a494273b10d5c5f62458d92 |
| Source note | uspto-grants-1983_10 |