HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[2-(Benzyloxy)-5-(pyridine-2-carbonyl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [3-Amino-4-(benzyloxy)phenyl](pyridin-2-yl)methanone | HCID 53880974 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[2-(Benzyloxy)-5-(pyridine-2-carbonyl)phenyl]acetamide | HCID 53916260 | — |
Reaction Steps
A mixture of 10.0 g (32.8 mmol) of 3-amino-4-benzyloxyphenyl 2-pyridyl ketone and 40 ml of acetic anhydride is heated on a steam bath for 1 hour. The reaction is concentrated in vacuo to give a residue which is suspended in water and made basic with 10% NaOH. The aqueous phase is extracted with ether and the dried extracts are evaporated to give 3-acetamido-4-benzyloxyphenyl 2-pyridyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985887 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-f3f9ebe34c5548768718f41339eb1228 |
| Source note | uspto-grants-1976_10 |