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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 620555생성일: 2026년 10월 24일

Diisopropylamine → Methyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propanoate

https://huagongshe.com/ko/reaction/620555

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Methyl methoxyacetateHCID 80507—
반응물2-(8-Phenyloctyl)benzaldehydeHCID 9817613—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propanoateHCID 15617503—

반응 단계

To tetrahydrofuran (50 ml), cooled to -78° C. under argon, was added diisopropylamine (5.7 ml, 0.041 mole) followed by n-butyllithium (16 ml, 0.041 mole) slowly. After 15 minutes, methyl methoxyacetate (4.25 g, 0.041 mole) in tetrahydrofuran (10 ml) was added dropwise. The resulting solution was stirred for 30 minutes after which a solution of 2-(8-phenyloctyl)benzaldehyde in tetrahydrofuran (10 ml) was added dropwise. After 2 hours the reaction mixture was quenched with a solution of saturated ammonium chloride and then diluted with ice water. The aqueous layer was extracted with ether. The combined ether extract was washed with 10% sodium hydroxide (ice cold), dried over magnesium sulfate, filtered and evaporated to give the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04820719
출처 데이터셋uspto-grants-1989_04
ORD IDord-0724cb3f0f4846d9b77d89be54ee01c4
출처 메모uspto-grants-1989_04