HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 964618Erstellt: 25. Oktober 2026
Sodium Iodide → 1-(3-Nitro-4-phenylmethoxyphenyl)ethanone
https://huagongshe.com/reaction/964618
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Hydroxy-3-Nitroacetophenone | HCID 138723 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-(3-Nitro-4-phenylmethoxyphenyl)ethanone | HCID 11265720 | 84% |
Reaktionsschritte
To a mechanically stirred DMF (260 mL) suspension of 1-[4-hydroxy-3-nitrophenyl]ethanone (51 g, 282 mmol) and K2CO3 (17 g, 847 mmol) was added benzyl bromide (68 mL, 572 mmol) followed by NaI (47 g, 313 mmol). After stirring overnight at 20° C., an additional 10 mL of benzyl bromide was added and the reaction was stirred for 15 more minutes. The reaction was quenched by the addition of 1.6 L water. The resulting suspension was stirred overnight and then filtered. The collected solids were washed 3×250 mL=750 mL water and dried in vacuo at ~55° C. to give 75 g crude product which was slurried in 1.3 L toluene at ~75° C., filtered hot through a 5.0 μm membrane, concentrated in vacuo to a volume of ~300 mL, diluted with 250 mL heptane, and the suspension cooled from ~60° C. to ambient. After filtration, the collected solids were washed with heptane and dried in vacuo at ~55° C. to give 64 g (84%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05770615 |
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| Quelldatensatz | uspto-grants-1998_06 |
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| ORD ID | ord-a1277345ecd2461dafe9eaf0610e5c60 |
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| Quellennotiz | uspto-grants-1998_06 |
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