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HRID 15003作成日:2026年10月27日

2,6-Lutidine → ((1-(4-Bromophenyl)hexyl)oxy)(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/15003

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-LutidineHCID 7937—
反応物tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
反応物Sodium BicarbonateHCID 516892—
反応物1-(4-Bromophenyl)hexan-1-olHCID 12603086—
溶媒DichloromethaneHCID 6344—
生成物((1-(4-Bromophenyl)hexyl)oxy)(tert-butyl)dimethylsilaneHCID 5743897388.4%

反応手順

TBSOTf (2.9 mL, 12.6 mmol) was added to an ice-cold solution of 4 (3.017 g, 11.7 mmol) and 2,6-lutidine (1.6 mL, 13.7 mmol) in dichloromethane (30 mL). The reaction was stirred for 2 h at room temperature and then 100 mL saturated sodium bicarbonate solution was added. The resulting mixture was extracted with dichloromethane (30 mL) and the dichloromethane layer was washed with 1 M HCl (2×50 mL) and brine (50 mL). The dichloromethane solution was then dried (MgSO4), filtered and evaporated. Purification of the residue by flash chromatography on silica gel (hexanes) gave compound 5 (3.843 g, 88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732443B2
出典データセットuspto-grants-2010_06
ORD IDord-57b752c626fb4e7bb2cebf81a4fdcceb
出典メモuspto-grants-2010_06