HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372369Generated: October 30, 2026
4-Nitrobenzaldehyde → 1,2-Bis(4-nitrophenyl)ethanone
https://huagongshe.com/reaction/2372369
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12240723 | HCID 12240723 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Bis(4-nitrophenyl)ethanone | HCID 12240724 | 95.7% |
Reaction Steps
A solution of KOH (7.56 g, 0.13 mol) in MeOH (75 ml) was added to the phosphonate ester 33 (62.1 g, 0.13 mol) in THF (400 ml) at -78° C. for 0.5 hour and p-nitrobenzaldehyde (20.3 g, 0.13 mol) in 200 ml of THF was added over 0.5 hour. The reaction was warmed to room temperature and stirred an additional 2 hours. THF was removed under reduced pressure. The residue was taken up in EtOAc and washed twice with 5% aqueous NaHCO3 and once with brine. The ethyl acetate was removed under reduced pressure. The dark red enemine was dissolved in CH3OH (600 ml) and concentrated HCl (0.2 ml) was added. The solution was stirred for 1 hour at room temperature and diluted with H2O (500 ml). The solid was filtered, washed with ether and dried to afford 34 (35.6 g, 82.0%), m.p. 131°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098918 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-ef995545ee344040b997866794cd2f2f |
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| Source note | uspto-grants-1992_03 |
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