Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylaniline | HCID 7515 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11499576 | HCID 11499576 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70194865 | HCID 70194865 | — |
Reaction Steps
3-(3,4-Difluorophenyl)glutaric anhydride (3.61 g) in CH2Cl2 (75 mL) at 0° C. was treated sequentially with N-methylaniline (2.16 mL), triethylamine (2.78 mL) and N,N-dimethylaminopyridine (195 mg). The mixture was stirred at 0° C. for two hours then allowed to warm to room temperature and stirred for 12 hours. The reaction mixture was diluted with CH2Cl2 (300 mL) and washed with 1N HCl (1×100 mL) and water (1×100 mL). The organic layers were dried over MgSO4, filtered and concentrated to afford the title compound (4.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654316 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-01b94f0a0e5c4309a019ec8ffc5a55e8 |
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| Source note | uspto-grants-1997_08 |
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