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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1073973생성일: 2026년 10월 26일

Benzaldehyde → alpha-Phenyl-N-(1,2,2,6,6-pentamethylpiperidin-4-yl) nitrone

https://huagongshe.com/reaction/1073973

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물1,2,2,6,6-Pentamethyl-piperidin-4-one oximeHCID 241950—
생성물alpha-Phenyl-N-(1,2,2,6,6-pentamethylpiperidin-4-yl) nitroneHCID 73159783—

반응 단계

Following the general procedure of Example 1, the title compound is prepared from 5.0 g (29.4 mmol) of 1,2,2,6,6-pentamethylpiperidin-4-one oxime and 3.1 g [29 mmol) of benzaldehyde in a yield of 2.3 g (30%) of a white solid which after recrystallization from heptane melts at 104°-105° C. 1HMR (200 MHz, CDCl3)δ 8.26 (m, 2H's); 7.45 (s, 1H); 7.40 (m, 3H's); 4.18 (tt, IH); 2.28 (s, 3H's); 2.13 (t, 2H's); 1.93 (dd, 2H's); 1.23 (s, 6H's); 1.10 (s, 6H's). IR (CDCl3) 3020, 2950, 1570, 1550,

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04972009
출처 데이터셋uspto-grants-1990_11
ORD IDord-e07e68c3b14f4afeb76110eca04025c2
출처 메모uspto-grants-1990_11