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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1416178Erstellt: 26. Oktober 2026

3-Methoxybenzenethiol → 6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran

https://huagongshe.com/reaction/1416178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-MethoxybenzenethiolHCID 84989—
Edukt6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyranHCID 14956089—
EduktSodium t-butoxideHCID 23676156—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelEthanolHCID 702—
Produkt6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyranHCID 1878287689,8%

Reaktionsschritte

6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyran (6.5 g) (see Preparation 4) was dissolved in absolute ethanol (135 ml), then sodium tert-butoxide (7.5 g), 3-methoxybenzenethiol (3.6 g) and tetrakis(triphenylphosphine)palladium(O) (0.35 g) were added and the mixture was heated under reflux under a nitrogen atmosphere for 48 hours. Further tetrakis(triphenylphosphine)palladium(O) (0.3 g) was added and heating was continued for a further 48 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane and washed with water. The organic layer was dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the crude product chromatographed on silica using 1:1 hexane: dichloromethane as the eluent to yield 6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (7.2 g) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05912244
Quelldatensatzuspto-grants-1999_06
ORD IDord-93d3b7e6ae6c47ad8c7c63f53a437795
Quellennotizuspto-grants-1999_06