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HRID 274025Erstellt: 26. Oktober 2026

Benzeneacetic acid, 3,4-dimethoxy-, methyl ester → alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester

https://huagongshe.com/reaction/274025

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneacetic acid, 3,4-dimethoxy-, methyl esterHCID 85213—
EduktSodiumHCID 5360545—
Edukt2,3-dihydro-6-methoxy-1H-isoindol-5-olHCID 10241135—
Edukt(5-Bromopentyl)(1,1-dimethylethyl)dimethyl silaneHCID 19042078—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl esterHCID 54212729—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution, -78° C. under argon, of 2 38 g of 3,4-dimethoxyphenyl acetic acid methyl ester in 30 ml of tetrahydrofuran is added 12.45 ml of 1.0M sodium hexamethylsidilazide. The solution is stirred at -78° C. for 5 minutes and then warmed to 0° C. for 1 hour. To this solution is added 3.5 g of (5-bromopentyl)(1,1-dimethylethyl)dimethyl silane. The reaction mixture is allowed to warm to room temperature and stirred for 12 hours. The mixture is diluted with diethyl ether and water, the layers are separated and the organic layer is washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: hexane/ethyl acetate,5/1) to give 2.6 g of the desired product as a clear oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387685
Quelldatensatzuspto-grants-1995_02
ORD IDord-278b8b799112408cad48b628991a6464
Quellennotizuspto-grants-1995_02