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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 862755Erstellt: 24. Oktober 2026

Iodine → HCID 23293626, Verbindung

https://huagongshe.com/de/reaction/862755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktEthyl bromoacetateHCID 7748—
Edukt6-Fluoro-1-indanoneHCID 1519464—
KatalysatorZincHCID 23994—
LösungsmittelBenzene etherHCID 22174802—
ProduktHCID 23293626HCID 2329362697%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05719186
Quelldatensatzuspto-grants-1998_02
ORD IDord-43e1f15fe6a143ef945e745c2b4e2794
Quellennotizuspto-grants-1998_02