Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylbenzeneethanamine | HCID 11503 | — |
| Reactant | 4-(3,4-Dichlorophenyl)oxane-2,6-dione | HCID 54363942 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19029352 | HCID 19029352 | — |
Reaction Steps
3-(3,4-Dichlorophenyl)glutaric anhydride (3.4 g) in CH2Cl2 (50 mL) at 0° C. was treated sequentially with N-methylphenethylamine (2.4 mL), triethylamine (2.3 mL) and N,N-dimethylaminopyridine (162 mg). The mixture was stirred at 0° C. for two hours then allowed to warm to room temperature and stirred for 20 hours. The reaction mixture was washed with 1N HCl (1×100 mL) and brine (1×100 mL). The organic layers were dried over MgSO4, filtered and concentrated to afford the title compound (4.6 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-c18d68c3d2c345df9eaf92c998f99cb3 |
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| Source note | uspto-grants-1997_08 |
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