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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25783생성일: 2026년 10월 24일

Water → 4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/25783

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Butene, 1-bromo-HCID 122414—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물4-(1-hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 20760332—
용매Dimethyl SulfoxideHCID 679—
생성물4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 2076033173.2%

반응 단계

A mixture of 70 mg of 4-(1-hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester in 2 mL of DMSO was treated with 0.22 mL of 1.0 M sodium bis(trimethylsilyl)amide and 29 mg of crotyl bromide at room temperature. The reaction mixture was allowed to stir at room temperature overnight. The reaction was worked up by adding water and extracted with EtOAc three times. The organic layers were combined, washed sequentially with saturated aqueous sodium bicarbonate solution, water, and brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography to yield 58 mg of 4-{1-[((E)-but-2-enyl)oxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858627B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-98eef52007ea4f0caa6af926eb09b25a
출처 메모uspto-grants-2005_02