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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430Erstellt: 23. Oktober 2026

1-(Benzyloxy)-3-bromobenzene → 2-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole

https://huagongshe.com/de/reaction/430

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
Edukt2-Methyl-6-(trifluoromethoxy)-1H-indoleHCID 12180669—
ReagenzSodium t-butoxideHCID 23676156—
Katalysator2-(Di-tert-butylphosphino)biphenylHCID 2734215—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt2-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indoleHCID 5921672062,48%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

EN04773-54, _Buchwald coupling, toluene and bromide_ The indole from 4773-41, 1-(benzyloxy)-3-bromobenzene,Pd2(dba)3 (5mol%), JohnPhos (10mol%) and KOtBu (1.4eq) were dissolved in toluene. The mixture was warmed at 80 °C for 40 hours.* The reaction was carefully monitored and analysis data from 2h, 4, 16 and 40 h are attached. According to LCMS there were ca 75% conversion to the product. The mixture was washed with water, concentrtaed and purified by silica column (Hep/EtOAc 6:1). The collected fractions contained product (6 g, 62.5% yield) but had some impurity (see TLC and NMR). Nevertheless Friedel crafts acylation was performed without further purifications. See e.g. 4773-56. ### *JohnPhos, pd2(dba)3 and sodium tertbutoxide had been dissolved in toluene and was portionwise added to the reaction mixture during the first 16h.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-f89f3a46444e42c0973a5acc34e50e60
Quellennotiz750 AstraZeneca ELN dataset