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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 575431Erstellt: 24. Oktober 2026

Iodine → HCID 89754670, Verbindung

https://huagongshe.com/de/reaction/575431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktStannaneHCID 123161—
EduktHCID 86693513HCID 86693513—
EduktHCID 89754796HCID 89754796—
LösungsmittelChloroformHCID 6212—
ProduktHCID 89754670HCID 8975467045%

Reaktionsschritte

To a rapidly stirred solution of crude of 3-fluoro-2-(trimethylstannyl)-6,7-dihydro-5H-5,7-methanobenzo[7]annulen-8(9H)-one (3.09 g at 37% purity LCMS-UV215) in chloroform (20 mL) at room temperature was introduced dropwise a solution of iodine (1.488 g, 5.86 mmol, 1.0 equivalent with respect to number of moles 5-bromo-4-fluorotricyclo[8.1.1.02,7]dodeca-2(7),3,5-trien-9-one used for stannane synthesis in previous synthetic step, as a saturated solution in chloroform). Following addition of the iodine solution, the reaction mixture was evaporated directly onto silica gel in vacuo. The dry-loaded material was purified by silica gel flash column chromatography (eluent: heptane/ethyl acetate gradient) to furnish the title compound (0.835 g, 2.64 mmol, 45% over 2 steps) as a yellow oil: 1H NMR (500 MHz, CDCl3) δ 2.08-2.14 (m, 2H), 2.87-2.96 (m, 2H), 3.22-3.28 (m, 1H), 3.48 (td, J=8.28, 3.63 Hz, 1H), 4.11 (s, 2H), 6.78 (d, J=8.51 Hz, 1H), 7.53 (d, J=6.31 Hz, 1H); M+H=317

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034866B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-69a12fef8e944fc3bb07bc8d1e539d28
Quellennotizuspto-grants-2015_05