Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(3,4-Dichlorophenyl)oxane-2,6-dione | HCID 54363942 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19029312 | HCID 19029312 | — |
Reaction Steps
3-(3,4-Dichlorophenyl)glutaric anhydride (10 g, Example 1, Step C) in CH2Cl2 (150 mL) at 0° C. was treated sequentially with o-anisidine (6 mL), triethylamine (6.7 mL) and N,N-dimethylaminopyridine (440 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 (500 mL) and washed with 1N HCl (1×200 mL) and water (1×200 mL). The organic layers were dried over MgSO4, filtered and concentrated to afford the title compound (14 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-bb153de115a84d40b8d456922e79f6d6 |
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| Source note | uspto-grants-1997_08 |
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