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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25791생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/25791

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참여 물질

역할이름HCID투입량
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물6-(2-Methoxyphenyl)-2,2-dimethyl-4-(1-phenethyloxyethyl)-1,2-dihydroquinoline 4-(1-Hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 69152501—
용매Phenethyl bromideHCID 7666—
용매TetrahydrofuranHCID 8028—
생성물4-{1-[(2E)-but-2-en-1-yloxy]ethyl}-6-(2-methoxyphenyl)-2,2-dimethyl-1,2-dihydroquinolineHCID 10316670140.4%

반응 단계

6-(2-Methoxyphenyl)-2,2-dimethyl-4-(1-phenethyloxyethyl)-1,2-dihydroquinoline 4-(1-Hydroxyethyl)-6-(2-methoxyphenyl)-2,2-dimethyl-2H-quinoline-1-carboxylic acid tert-butyl ester (100 mg) was treated with 360 μL of 1 M solution of sodium bis(trimethylsilyl)amide in THF and 45 μL of phenethyl bromide to give the alkylated product, which was deprotected to yield 62 mg of the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858627B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-f7d5dd04ee0f424a9cdb3a8acaf6d5c2
출처 메모uspto-grants-2005_02