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HRID 1980512Erstellt: 26. Oktober 2026

Imidazole → Chloromethyl(1,1-dimethylethoxy)methyl(phenyl)silane

https://huagongshe.com/reaction/1980512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
EduktChloro(chloromethyl)methyl(phenyl)silaneHCID 12418873—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktChloromethyl(1,1-dimethylethoxy)methyl(phenyl)silaneHCID 1347459576,9%

Reaktionsschritte

A mixture of 15.4 g (0.075 mol) of chloro(chloromethyl)methyl(phenyl)silane, 14 ml (11.1 g, 0.15 mol) of t-butanol, 11.5 ml (8.3 g, 0.082 g) of triethylamine, and 0.5 g (0.008 mol) of imidazole in 60 ml of dimethylformamide was stirred at 80° For 2 hours. The resulting slurry was cooled, poured into 200 ml of water, and extracted with ether. The ether extracts were washed three times with water, followed by 0.1N aqueous HCl, saturated aqueous NaHCO3, and brine dried over magnesium sulfate, and evaporated to leave 14.0 g of a pale orange oil. Distillation provided 11.9 g (65%) of the title compound: bp 78°-82° (0.2 mm); nD21 1.5010; ir (neat) 3080, 3060, 2990, 2940, 1600, 1435, 1395, 1370, 1260, 1245, 1195, 1125, 1060, 1030, 815, 790, 740, 725, 705, 650 cm-1 ; nmr (CDCl3): 0.5 (3H, s), 1.3 (9H, s), 2.9 (2H, s) and 7.3-7.8 (5H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04510136
Quelldatensatzuspto-grants-1985_04
ORD IDord-84f386f9a72648a388f8546763acfd46
Quellennotizuspto-grants-1985_04