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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 2-Phenylchroman-6-ol | HCID 21287538 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 2-Nitro-1-(2-phenylchroman-6-yloxy)-benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425568B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-d43da5d2175a43c7bb5ecbd4fc202682 |
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| Quellennotiz | uspto-grants-2008_09 |
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