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HRID 1023326作成日:2026年10月27日

Iodine → 1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-ol

https://huagongshe.com/reaction/1023326

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Propylene OxideHCID 6378—
反応物Ammonium ChlorideHCID 25517—
反応物4-Bromobenzyloxy-tert-butyldimethylsilaneHCID 10859583—
溶媒TetrahydrofuranHCID 8028—
生成物1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-olHCID 67377030—

反応条件

温度50 °C

反応手順

To a solution of (4-bromobenzyloxy)(tert-butyl)dimethylsilane (3.080 g) in THF (20 mL) were added Mg (0.288 g) and I2 (cat) at room temperature under an Ar atmosphere. The mixture was heated at 50° C. for 1 hour, and then cooled to room temperature. To the mixture was added 1,2-epoxypropane (0.77 mL) at room temperature under an Ar atmosphere, and the mixture was stirred at room temperature for 14.5 hours, and then heated at 50° C. for 1 hour, and then cooled to room temperature. To the mixture was added saturated aqueous NH4Cl, and the mixture was extracted with AcOEt. The organic layer was washed with saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=2/1) to afford 1-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-ol (1.485 g) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722663B2
出典データセットuspto-grants-2014_05
ORD IDord-3bbe2a901c9b43e794b12ea9324b81fc
出典メモuspto-grants-2014_05