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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2353511Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2353511

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
PatentnummerUS07750039B2
Quelldatensatzuspto-grants-2010_07
ORD IDord-66360f14f0e747f085b29b561ef1748e
Quellennotizuspto-grants-2010_07