HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → Methyl-2-methoxy-5-benzamidobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 5-amino-o-anisate | HCID 89843 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl-2-methoxy-5-benzamidobenzoate | HCID 22620052 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 9.92 grams (55 mmol) of methyl-2-methoxy-5-aminobenzoate was taken up in 250 ml methylene chloride, treated with 8.4 mL (61 mmol) triethylamine and cooled to 0° C. The reaction mixture was then treated with 8.1 grams (57 mmol) benzoyl chloride in a dropwise fashion. The reaction mixture was stirred for 30 minutes while warming to room temperature. The reaction mixture was diluted with 500 mL of methylene chloride, washed with 200 mL saturated bicarbonate solution and then rewashed with water and brine. The organic phase was dried and evaporated to a flaky white solid (15.7 grams). This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06369074B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-ac97a016dea644448e4169f99f7faaeb |
| Source note | uspto-grants-2002_04 |