HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-acetoxymethyl-5-methoxy-N-(3-pyridylmethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-hydroxymethyl-5-methoxy-N-(3-pyridylmethyl)benzamide | HCID 20082005 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-acetoxymethyl-5-methoxy-N-(3-pyridylmethyl)benzamide | HCID 20082003 | 100% |
Reaction Steps
A solution of 710 mg of 2-hydroxymethyl-5-methoxy-N-(3-pyridylmethyl) benzamide and 317 mg of triethylamine in 10 ml of methylene chloride was chilled at 0° C., mixed with 320 mg of acetic anhydride and stirred at room temperature for 15 hours. The reaction mixture was washed with water and saturated brine in order. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo to give 820 mg of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05304556 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-417f44e2e8774e5bb426b3d89b2514ab |
| Source note | uspto-grants-1994_04 |