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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25786생성일: 2026년 10월 24일

Bromomethylstyrene → 4-{1-[(2E)-but-2-en-1-yloxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinoline

https://huagongshe.com/ko/reaction/25786

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참여 물질

역할이름HCID투입량
반응물BromomethylstyreneHCID 98116—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물6-(2-Methoxyphenyl)-2,2-dimethyl-4-[1-((E)-3-phenylallyloxy)ethyl]-1,2-dihydroquinoline 4-(1-Hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 69153346—
용매TetrahydrofuranHCID 8028—
생성물4-{1-[(2E)-but-2-en-1-yloxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinolineHCID 1031667019%

반응 단계

6-(2-Methoxyphenyl)-2,2-dimethyl-4-[1-((E)-3-phenylallyloxy)ethyl]-1,2-dihydroquinoline 4-(1-Hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester (70 mg) was treated with 255 μL of 1 M solution of sodium bis(trimethylsilyl)amide in THF and 50 mg of cinnamyl bromide to give the alkylated product, which was deprotected to yield 5.8 mg of the title compound as a foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858627B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-9de8337d60034e7caad34f64ccdae3ce
출처 메모uspto-grants-2005_02