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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21616생성일: 2026년 10월 24일

Tetrahydrofuran → Diethyl alpha-(3.5-di-tert-butyl-4-methoxyphenyl)-N-(3-phenylpropyl)-aminomethylphosphonate

https://huagongshe.com/ko/reaction/21616

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물3-PhenylpropylamineHCID 16259—
반응물DiethylphosphiteHCID 3780918—
반응물3,5-DI-Tert-butyl-4-methoxybenzaldehydeHCID 12910939—
생성물Diethyl alpha-(3.5-di-tert-butyl-4-methoxyphenyl)-N-(3-phenylpropyl)-aminomethylphosphonateHCID 13171902337%

반응 단계

This aldehyde was reacted with 0.63 g (4.68 mmol) 3-phenylpropylamine in 25 ml THF, then 0.65 g (4.68 mmol) diethylphosphite was added and the resulting mixture heated at i10° C. for 4 h. Purification by column chromatography gave 0.9 g (37% of a yellow oil). IR (film) 3400 cm-1 (broad): NH, 1440: tert-Bu, 1220: P=O, 1020: P--O--C. NMR (CDCl3): δ=7.24 and 7.14 (2 m, 5H) phenyl H 7.26 (d, JP-H =2 Hz, 2H): aromatic H, 3,5 di-tert-butyl-4-hydroxyphenyl 4.05, 3.93 and 3.79 (3 m, 4H): P--O--CH2 --CH3 3.95 (d, JP-H =19 Hz, 1H): CH--PO3ET2 3.66 (s, 3H): Ph--O--CH3 2.66 and 2.59 (2 m, 4H): NH--CH2 --CH2 --CH2 --Ph 1.79 (m, 3H): NH and NH--CH2 --CH2 --CH2 --Ph 1.42 (s, 18H): tert-Bu 1.27 and 1.10 (2t, J=7 Hz, 6H): P--O--CH2 --CH3MS: m/e=504: M+ +366:M+ --PO3Et2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424303
출처 데이터셋uspto-grants-1995_06
ORD IDord-b3248921defb4c6a8d30d19c0d84be8d
출처 메모uspto-grants-1995_06