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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227409Erstellt: 23. Oktober 2026

6-(benzyloxy)-1H-indole → (6-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone

https://huagongshe.com/de/reaction/227409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-(benzyloxy)-1H-indoleHCID 260804—
Edukt2,2,3,3-Tetramethylcyclopropane-1-carbonyl chlorideHCID 11041002—
EduktHCID 178418443HCID 178418443—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelDichloromethaneHCID 6344—
Produkt(6-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanoneHCID 2482378064,4%

Reaktionsschritte

A mixture of 6-benzyloxyindole (Lancaster, 2.0 g, 9.0 mmol), ethylmagnesium bromide (1.0 M solution in THF, 11 mL, 11 mmol), zinc chloride (1.0 M solution in Et2O, 11 mL, 11 mmol) and the product of Example 1A (13.4 mmol) in 30 mL of dichloromethane was processed as described in Example 1B to provide the title compound (2.0 g, 5.8 mmol, 64% yield). MS (DCI/NH3) m/z 348 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560481B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-0200d6e4d77a485a8470521c8d7eb478
Quellennotizuspto-grants-2009_07