HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-nitro-4-[(E)-2-nitroethenyl]benzene → (1R,2R,3R,4S)-ethyl 4-((ethoxycarbonyl)methyl)-1-acetyl-3-nitro-2-(4-nitrophenyl)cyclopentanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-nitro-4-[(E)-2-nitroethenyl]benzene | HCID 5355016 | — |
| Reactant | Diethyl 5-acetylhex-2-enedioate | HCID 85439255 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1R,2R,3R,4S)-ethyl 4-((ethoxycarbonyl)methyl)-1-acetyl-3-nitro-2-(4-nitrophenyl)cyclopentanecarboxylate | HCID 59592087 | 81% |
Reaction Steps
To a solution of diethyl 5-acetylhex-2-enedioate (4a, 0.3 mmol, 1.0 eq) and 1-nitro-4-((E)-2-nitrovinyl)benzene (0.6 mmol, 2.0 eq) in diethyl ether (0.4 mL) was added catalyst VI (Q-NH2) (0.06 mmol, 0.2 eq) at room temperature (22° C.). The resulting mixture was stirred vigorously for 24 hours, then the reaction was continued for about 6 hours after removal of the solvent. After the reaction was completed (monitored by TLC and crude NMR), the title product was afforded by flash chromatography over silica gel (Et2O:Hexane=1:10 to 1:3) in 81% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754252B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-df82081f317d4f62ad0e1a23c8dd21fe |
| Source note | uspto-grants-2014_06 |