HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Methyl 5-acetamido-2-bromobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 5-amino-2-bromobenzoate | HCID 245495 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-acetamido-2-bromobenzoate | HCID 58891822 | 98% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Methyl 5-amino-2-bromobenzoate (Reference Compound No. 1-(1), 21.0 g, 91.2 mmol) was dissolved in anhydrous dichloromethane (450 mL), triethylamine (19.0 mL, 137 mmol) and acetyl chloride (13.0 mL, 182 mmol) were added dropwise over 30 minutes successively, and then the mixture was stirred at 0° C. for 2 hours. The reaction mixture was washed with water (200 mL, 2 times), saturated aqueous sodium hydrogen carbonate solution (200 mL, 2 times), and saturated brine (200 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was filtered with hexane-ethyl acetate (20:1) to give the titled reference compound (24.2 g) as a pale yellow solid. (Yield 98%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975256B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-4c8ed155e9e14899836e0c1be4cb74e6 |
| Source note | uspto-grants-2015_03 |