HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088189Generated: November 3, 2026
4-Nitrobenzaldehyde → HCID 23912199, compound
https://huagongshe.com/reaction/1088189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzeneacetonitrile, 4-methoxy- | HCID 66031 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23912199 | HCID 23912199 | 6.5% |
Reaction Steps
4-Methoxyphenylacetonitrile (7.63 g, 50 mmol) in toluene (30 mL), PEG(E)-400 (4 g, 10 mmol) and 52% aqueous sodium hydroxide (10.73 g in 12.4 mL water) were placed in a flask equipped with a magnetic stirrer. 4-Nitrobenzaldehyde (7.56 g, 50 mmol) in a minimum of toluene was added dropwise. The mixture was stirred for 1 h at 20° C. and then diluted with water (30 mL). The organic layer was separated, washed with water (3×40 mL) and dried with sodium sulfate. The solvent was removed under reduced pressure and the residue was recrystallized from toluene at -20° C. to give 1-cyano-1-(4-methoxyphenyl)-2-(4-nitrophenyl)ethylene (yield=0.913 g, 6.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04961631 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-f6e1151de07b4f1a86ee28cd780689e3 |
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| Source note | uspto-grants-1990_10 |
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