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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31225Erstellt: 24. Oktober 2026

Dichloromethane → 2-Nitro-1-(2-phenylchroman-6-yloxy)-benzene

https://huagongshe.com/de/reaction/31225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1-Chloro-2-nitrobenzeneHCID 6945—
EduktPotassium HydroxideHCID 14797—
Edukt2-Phenylchroman-6-olHCID 21287538—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt2-Nitro-1-(2-phenylchroman-6-yloxy)-benzeneHCID 17978475—

Reaktionsschritte

6-Hydroxyflavane (0.150 g) was dissolved in dry DMSO (5 ml) under nitrogen. KI (0.166 g) and KOH (0.074g) were added and solution was stirred at room temperature for 15 minutes. 2-Chloro-1-nitrobenzene (0.104 g) was added and the solution was stirred at +90° C. for 2.5 hours. Cooled solution was taken up with CH2Cl2 and washed with H2O and 2M NaOH. Phases were separated and water phase was washed CH2Cl2. All organic phases were combined and washed with 1M HCl and then H2O (until pH˜7) and brine. Solution was dried over Na2SO4 and purified with filtration through the small silica column in CH2Cl2:n-heptane (60:40). 1H-NMR (300 MHz; d6-DMSO): δ 8.01 (dd, 1H, J=8.1 Hz; J=1.7 Hz), 7.69 (m, 1H), 7.50-7.31 (m, 5H), 7.31-7.24 (m, 1H), 7.04 (dd, 1H, J=8.5 Hz; J=1.2 Hz), 6.92 (s, 1H), 6.90 (s, 2H), 5.12 (dd, 1H, J=10.1 Hz; J=2.3 Hz), 2.95 (ddd, 1H, J=16.9 Hz; J=11.2 Hz, J=5.8 Hz), 2.73 (ddd, 1H, J=16.9 Hz; J=3.2 Hz, J=1.7 Hz), 2.25-2.10 (m, 1H), 2.08-1.90 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425568B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-d43da5d2175a43c7bb5ecbd4fc202682
Quellennotizuspto-grants-2008_09