HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 322609Erstellt: 24. Oktober 2026
1,2-Dibromoethane → Benzene, 2-(2-bromoethoxy)-4-methyl-1-nitro-
https://huagongshe.com/de/reaction/322609
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dibromoethane | HCID 7839 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 6-Nitro-m-cresol | HCID 12788 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Benzene, 2-(2-bromoethoxy)-4-methyl-1-nitro- | HCID 13685252 | 115,3% |
Reaktionsschritte
122.5 g (800 mmol) 5-methyl-2-nitrophenol, 751.0 g (4000 mmol) 1,2-dibromoethane, 110.7 g (800 mmol) K2CO3 were suspended in 400 ml anhydrous DMF. The suspension was heated at 120° C. for 1 hour, then cooled and most of the liquid was evaporated. The residue was dissolved in 1 l CHCl3 and 1 l water. The organic layer was washed with 2×1 l of 1.8% NaOH till the aqueous layer became pale yellow. The organic layer was dried over Na2SO4 for 18 h, filtered and the solvent was evaporated to give ˜240 g oil. The oil was triturated with 240 ml boiling methanol and allowed to settle for 2 h. The resultant precipitate was filtered, washed with 2×100 ml cold methanol and dried at RT for 18 h to afford 89.4 g (43%) off-white crystal. H1NMR (CDCl3) δ (ppm): 2.40(s, 3H), 3.65(t,2H), 4.30(t,2H), 6.85(d,2H), 7.75(d,1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06211359B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-e281d559eef24698a3ec34a00625fabe |
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| Quellennotiz | uspto-grants-2001_04 |
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