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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223645생성일: 2026년 10월 25일

Benzylamine → 3-Ethyl-3-n-butyl-12-phenyl-1-aza-1,5,9-cyclododecatriene

https://huagongshe.com/reaction/223645

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물2-Ethylhex-2-EnalHCID 12582—
반응물N-benzylidene-(2-ethyl-1-hexenylamine)HCID 56636874—
생성물3-Ethyl-3-n-butyl-12-phenyl-1-aza-1,5,9-cyclododecatrieneHCID 54523241—

반응 단계

The procedure described in Example 1(a) is repeated, except that 215.3 g (1 mol) of N-benzylidene-(2-ethyl-1-hexenylamine) [1-phenyl-4-ethyl-4-n-butyl-2-aza-1,3-butadiene; prepared by reacting benzylamine with 2-ethyl-hexenal and then isomerising the reaction product with potassium tert.-butylate; boiling point 90° C./7 Pa; nD20 =1.5630] are used. Distillation yields 288 g (0.891 mol) of 3-n-butyl-3-ethyl-12-phenyl-1-aza-1,5,9-cyclododecatriene; boiling point 130° C./2 Pa; nD20 =1.5296.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04355177
출처 데이터셋uspto-grants-1982_10
ORD IDord-099217fb9a2d4c969136b0514f5ca373
출처 메모uspto-grants-1982_10