Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67036724 | HCID 67036724 | — |
| Reactant | 2-Bromo-1-(3,4-dimethoxy-5-nitrophenyl)ethanone | HCID 71445791 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 67037009 | HCID 67037009 | — |
Reaction Steps
To a stirred solution of 3-(3-ethoxy-3-oxopropanoyl)-2-(trifluoromethyl)pyridine-1-oxide (1.39 g, 5 mmol) in pyridine (25 mL) was added 2-bromo-1-(3,4-dimethoxy-5-nitrophenyl)ethanone (1.67 g, 5.5 mmol). The reaction mixture was heated to 70° C. and stirred for 5 hours, then cooled to room temperature and poured onto 6 N aqueous HCl (100 mL). The precipitate was filtered off, washed with water and dried over P2O5 under vacuum. The solid was recrystallised from dichloromethane/ispropanol to give crude 3-(4-(3,4-dimethoxy-5-nitrophenyl)-3-(ethoxycarbonyl)furan-2-yl)-2-(trifluoromethyl)pyridine 1-oxide, 1.05 g (43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168793B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-f1d720651a924342be89b44a3e8103c2 |
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| Source note | uspto-grants-2012_05 |
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