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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DibromoethaneHCID 7839—
EduktPotassium CarbonateHCID 11430—
Edukt6-Nitro-m-cresolHCID 12788—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzene, 2-(2-bromoethoxy)-4-methyl-1-nitro-HCID 13685252115,3%

Reaktionsbedingungen

Temperatur120 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211359B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-e281d559eef24698a3ec34a00625fabe
Quellennotizuspto-grants-2001_04