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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2273303생성일: 2026년 10월 26일

Triethylamine → 4-(tert-Butyldiphenylsilyloxymethyl)-1-(2-trimethylsilylethoxy methyl)-1H-imidazole

https://huagongshe.com/reaction/2273303

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물1-(2-Trimethylsilylethoxymethyl)-1H-imidazole-4-methanolHCID 69558376—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물4-(tert-Butyldiphenylsilyloxymethyl)-1-(2-trimethylsilylethoxy methyl)-1H-imidazoleHCID 71087293—

반응 단계

1-(2-Trimethylsilylethoxymethyl)-1H-imidazole-4-methanol (100 g, WO 01/02145) was dissolved in dichloromethane (1 L), and triethylamine (hereinafter sometimes referred to as TEA) (122 mL), 4-(N,N-dimethylamino)pyridine (hereinafter sometimes referred to as DMAP) (5.35 g) and tert-butyldiphenylsilyl chloride (hereinafter sometimes referred to as TBDPSCl) (149 mL) were added under stirring. After stirring for a day, the reaction mixture was washed with water and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resulting residue was purified by flash chromatography (ethyl acetate/hexane=25%→50%) using a silica gel column (trade name: Ultrapack E, manufactured by Yamazen Corporation) to give the title compound (146 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09120835B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-cc135a832b9343f7a4ab23eb361777f7
출처 메모uspto-grants-2015_09