Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 4-Cyclohexyloxybenzaldehyde | HCID 11287179 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59255256 | HCID 59255256 | 96% |
Reaction Steps
A mixture of 4-cyclohexyloxy-benzaldehyde (2.84 g, 13.9 mmol) described in Manufacturing Example 79-1-1, nitromethane (3.74 mL, 69.5 mmol), ammonium acetate (2.14 g, 27.8 mmol) and acetic acid (30 mL) was stirred for 14 hours at 100° C. This mixture was cooled to room temperature, concentrated under a reduced pressure, and diluted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (3.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507530B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-74a16d61772e44f280a99544bc3f76f1 |
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| Source note | uspto-grants-2013_08 |
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