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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1023326생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1023326

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Propylene OxideHCID 6378—
반응물Ammonium ChlorideHCID 25517—
반응물4-Bromobenzyloxy-tert-butyldimethylsilaneHCID 10859583—
용매TetrahydrofuranHCID 8028—
생성물1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-olHCID 67377030—

반응 조건

온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722663B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-3bbe2a901c9b43e794b12ea9324b81fc
출처 메모uspto-grants-2014_05