Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 46913783 | HCID 46913783 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 46913784 | HCID 46913784 | 56% |
Reaction Steps
A solution of HNO3 (65%, 3 mL) in Ac2O (2 mL) at 0° C. was slowly added with a suspension of the compound of Example 1 (1.1 g, 2.9 mmol) in Ac2O (3 mL). After stirring at 0° C. for 2 h, the reaction mixture was poured into 50 mL of ice/water and the precipitate was recovered by filtration. The resulting yellow solid was recrystallized with 95% EtOH (5 mL) to give 1-[(4-acetyl-2-methoxy-5-nitrophenoxy)methyl]-N-benzyloxycarbonyl-1-aminocyclopropane (0.69 g, yield: 56%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012645B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-a3cc80dc3156401781ab0a9edaafd74f |
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| Source note | uspto-grants-2015_04 |
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