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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25027Erstellt: 25. Oktober 2026

Chlorotrimethylsilane → N-(2,6-Dimethylbenzyl)phthalimide

https://huagongshe.com/reaction/25027

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
Edukt(2,6-Dimethylphenyl)methanolHCID 186748—
EduktPhthalimide potassium saltHCID 24194345—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(2,6-Dimethylbenzyl)phthalimideHCID 10825581—

Reaktionsschritte

To a stirred solution of 2,6-Dimethylbenzyl Alcohol (Step A, 6.59 g, 48.4 mmol) in DMSO (20 ml) was added chlorotrimethylsilane (15.75 ml, 145 mmol) at room temperature, and the mixture was stirred for one hr. To this reaction mixture were added ethyl acetate and water, the organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to give an oil. The oily residue was redissolved in DMF (100 ml) and potassium phthalimide (10.76 g, 58.1 mmol) was added. The reaction mixture was stirred for 16 hours at room temperature, ethyl acetate was added, and the organic layer was washed with 3% Na2CO3, 1 N HCl, dried over Na2SO4, filtered and concentrated to give white solid. The purification was done by flash chromatography on silica gel column (chloroform:methanol 95:5) to provide the title compound as white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858602B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-b39a908e70c044be99ef9823cba1f34d
Quellennotizuspto-grants-2005_02