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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234221Erstellt: 27. Oktober 2026

Triethylamine → 2-Formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester

https://huagongshe.com/reaction/234221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt2-Formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid allyl esterHCID 53735263—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl esterHCID 5381227993,8%

Reaktionsschritte

To a solution of 15 g of 2-formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid allyl ester in 0.12 l of N,N-dimethylformamide were added 13.8 g of tert-butyl-dimethylchlorosilane and 12.0 g of triethylamine. The mixture was stirred for 3 h at room temperature and then evaporated in vacuo. The residue was taken up in 0.4 l of ethyl acetate and the solution was washed successively with 1N hydrochloric acid, water and brine. The organic layer was dried over sodium sulfate. The solvent was evaporated in vacuo and the solid residue was recrystallized from hexane to give 20.5 g of 2-formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester as white crystals of m.p. 94°-95° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594135
Quelldatensatzuspto-grants-1997_01
ORD IDord-729178c747044f0bb42657ac8014b5bd
Quellennotizuspto-grants-1997_01