Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 66801851 | HCID 66801851 | 42.93% |
Reaction Steps
Nitro ethane (30.94 mL, 430.73 mmol) was added to 4-trifluoromethyl-benzaldehyde (5 g, 28.71 mmol) and ammonium acetate (6.64 g, 86.15 mmol) and the resulting mixture was refluxed at 115° C. overnight. The reaction was monitored by TLC (10% ethylacetate in hexane). The reaction mass was cooled and partitioned between ethylacetate and water. The organic layer was washed with water, brine solution, dried over anhydrous sodium sulphate and concentrated. Purification by column chromatography on silica gel (2% ethylacetate in hexane) afforded 2.85 g of the product (42.93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946260B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-da3f868b19fa48a6b333640eaa2fde44 |
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| Source note | uspto-grants-2015_02 |
|---|