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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347301생성일: 2026년 10월 24일

Diisopropylamine → HCID 12709724, 화합물

https://huagongshe.com/ko/reaction/347301

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물TetrahydrofuranHCID 8028—
반응물beta-nitrostyrene, (E)-HCID 5284459—
반응물ButyllithiumHCID 178418339—
생성물Lithium diisopropylamideHCID 2724682—
생성물HCID 12709724HCID 1270972484%

반응 조건

온도-20 °C

반응 단계

An LDA (14 mmol) solution was prepared by treating diisopropylamine (1.37 g, 14 mmol) with BuLi (1.6 M, 8.5 mL, 14 mmol) at −78° C. in dry THF (10 mL) under argon and allowing to warm up to −20° C. This solution was then cooled to −60° C. added to a solution of 1-benzyl-piperidine-4-ethyl carboxylate (3.05 g, 12 mmol) in THF (8 mL) at −60° C. and allowed to warm up to −40° C. over 1 h whereupon a solution of trans-beta-nitrostyrene (1.93 g, 13 mmol) in THF (8 mL) was added dropwise. The reaction mixture was allowed to warm up to room temperature over 1 h and then quenched with ammonium chloride (saturated, 40 mL) and the product extracted with ethyl acetate (2×40 mL). The combined organic extracts were then washed with brine, dried over sodium sulfate, filtered and evaporated. Purification by chromatography on silica gel eluting with DCM:MeOH (9:1) afforded the title compound (4.1 g, 84%) as a light yellow gum. MS: m/e=397.4 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173133B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-4cfcaf5e49ec43b695507a737ecaa876
출처 메모uspto-grants-2007_02