HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-Acetylamino-4'-methyl-biphenyl-3-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Methyl 5-amino-4'-methylbiphenyl-3-carboxylate | HCID 57850917 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Acetylamino-4'-methyl-biphenyl-3-carboxylic acid methyl ester | HCID 57851440 | — |
Reaction Steps
To a stirred solution of 5-amino-4′-methyl-biphenyl-3-carboxylic acid methyl ester (3.672 mmol, 884.9 mg) and pyridine (36.7 mmol, 3 mL) in 8 mL of dry CH2Cl2 was added acetic anhydride (7.3 mmol) at room temperature. The mixture was stirred at room temperature for 1 hour, then diluted with ethyl acetate (150 mL). The organic layer was washed with saturated aqueous CuSO4 solution, brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 5-acetylamino-4′-methyl-biphenyl-3-carboxylic acid methyl ester (quant. Yield), which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846945B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-13e082ccfe5d4b2fac35bac0f7e97979 |
| Source note | uspto-grants-2014_09 |