HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Allyl 5-acetamido-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Allyl 5-amino-2-nitrobenzoate | HCID 19432493 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Allyl 5-acetamido-2-nitrobenzoate | HCID 19432451 | 94.2% |
Reaction Steps
A solution of acetyl chloride (3.18 g, 40.5 mM) in dichloromethane (10 ml) under an argon atmosphere was added at 0° to a solution of allyl 5-amino-2-nitrobenzoate (3.0 g, 13.5 mM) in dichloromethane (30 ml). After addition of a solution of triethylamine (1.88 ml, 13.5 mM) in dichloromethane (10 ml) the mixture was stirred at ambient temperature overnight. The solvent was evaporated and the residue purified by chromatography on silica. Elution with ethyl acetate/petroleum ether (50/50) gave allyl 5-acetamido-2-nitrobenzoate (3.36 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541178 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-c827cefe88464077ba249dab731d45a9 |
| Source note | uspto-grants-1996_07 |