HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,6-Diiodohexane → 1,2-Dihydro-4-(6-iodohexyloxy)-1,2-dioxonaphthalene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,6-Diiodohexane | HCID 12373 | — |
| Edukt | HCID 178516607 | HCID 178516607 | — |
| Katalysator | Silver | HCID 23954 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 1,2-Dihydro-4-(6-iodohexyloxy)-1,2-dioxonaphthalene | HCID 22647794 | 57% |
Reaktionsschritte
A mixture of 1,6-diiodohexane (10.14 g, 30 mmol) and the silver salt of 2-hydroxy-1,4-naphthoquinone (2.81 g, 10 mmol) in benzene (60 mL) was stirred for 12 h at room temperature. The reacton mixture was filtered through Celite, concentrated in vacuo, and purified by flash chromatography (hexane/ EtOAc 4:1) to give a yellow solid (2,19 g, 57%); mp 85-87° C.; 1H NMR (CDCl3) 8.12 (dd, J=6.5, 1.0 Hz, 1H), 7.86 (dd, J=6.9, 0.9 Hz, 1H), 7.70 (dt, J=7.6, 1.5 Hz, 1H), 7.58 (dt, J=7.5, 1.3 Hz, 1H), 5.95 (s, 1H), 4.15 (t, J=6.3, 2H), 3.22 (t, J=6.9 Hz, 2H), 1.80-2.05 (m, 4H), 1.45-2.10 (m, 4H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06809176B2 |
| Quelldatensatz | uspto-grants-2004_10 |
| ORD ID | ord-d24a76d0339b435e93c6e92a67fccd61 |
| Quellennotiz | uspto-grants-2004_10 |