Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 23034795 | HCID 23034795 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86730326 | HCID 86730326 | 52% |
Reaction Steps
3-(Benzyloxy)-4-(difluoromethoxy)benzaldehyde described in Production Example 19-2 (3.94 g, 14.2 mmol) was dissolved in acetic acid (11 mL), then ammonium acetate (1.27 g, 16.4 mmol) and nitromethane (1.9 mL, 35.1 mmol) were added under nitrogen atmosphere at room temperature, and the mixture was heated and stirred at 130° C. for 2 hours. The mixture was cooled to room temperature and then heated and stirred at 130° C. again for 1 hour. The precipitate was collected by filteration and washed with a liquid mixture of acetic acid and ethanol to obtain the title compound (2.36 g, 52%). The filtrate was dissolved in dichloromethane and the resultant was purified with silica gel column chromatography (n-heptane:ethyl acetate=19:1-4:1), and then the target fraction was concentrated under vacuum. The precipitate was washed with ethanol to obtain the title compound (406 mg, 8.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933099B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-ff99f68533c64a299e06c0f8a983ac32 |
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| Source note | uspto-grants-2015_01 |
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