HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Iodine → HCID 23293626, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | 6-Fluoro-1-indanone | HCID 1519464 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Benzene ether | HCID 22174802 | — |
| Produkt | HCID 23293626 | HCID 23293626 | 97% |
Reaktionsschritte
A mixture of 6-fluoro-1-indanone (5.0 g, 33.3 mmol), ethyl bromoacetate (8.3 g, 50.0 mmol, Aldrich), activated zinc powder (3.2 g, 50.0 mmol, Mallinckrodt; Org. Synth., Coll. Vol. 6, 290, 1988) and a few crystals of iodine in diethyl ether-benzene (1:1, 100 mL) was heated at reflux under nitrogen for 24 h. The mixture was filtered and the filtrate was concentrated in vacuo. The residue in diethyl ether was vigorously stirred with excess dilute ammonium hydroxide, dried and concentrated to give ethyl 2-(6-fluoro-1-hydroxy-1-indanyl)acetate as an amber oil (7.6 g, 97%); NMR (DMSO-d6): d 6.99-7.24 (m, 3H, Ar), 5.38 (s, 1H, OH), 4.00 (q, 2H, CH2CH3), 2.64-2.92 (m, 4H, 2XCH2), 2.45-2.54, 2.05-2.14 (2m's, 2H, CH2CO), 1.08 (t,3H, CH3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05719186 |
| Quelldatensatz | uspto-grants-1998_02 |
| ORD ID | ord-43e1f15fe6a143ef945e745c2b4e2794 |
| Quellennotiz | uspto-grants-1998_02 |