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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31352Erstellt: 23. Oktober 2026

2-Bromoanisole → 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/de/reaction/31352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromoanisoleHCID 11358—
EduktAmmonium ChlorideHCID 25517—
Edukt5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dioneHCID 2732752—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-oneHCID 2190589976,3%
ProduktHCID 178489560HCID 178489560—

Reaktionsschritte

A solution of 2-methoxyphenylmagnesium bromide is prepared starting with 1.9 g of magnesium in 4 ml of ether and a solution of 14.54 g of 1-bromo-2-methoxybenzene in 21 ml of ether. This solution is added dropwise, under an argon atmosphere, to a mixture of 5 g of 5-trifluoromethoxy-1H-indole-2,3-dione in 26 ml of THF, precooled on an ice bath, the resulting mixture is then heated at the reflux temperature of the ether for 1 hour 30 minutes and is allowed to cool to RT. The reaction mixture is poured slowly into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with 5% K2CO3 solution, with water and with saturated NaCl solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. 2.8 g of the expected product are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425566B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-c0c9fcda8b5943aea3d4da63af3bb7f5
Quellennotizuspto-grants-2008_09