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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1658163생성일: 2026년 10월 25일

p-Toluenesulfonic acid → Benzonitrile, 4-(((4-hexylphenyl)methylene)amino)-

https://huagongshe.com/reaction/1658163

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-AminobenzonitrileHCID 13396—
반응물Benzaldehyde, 4-hexyl-HCID 170813—
용매BenzeneHCID 241—
생성물Benzonitrile, 4-(((4-hexylphenyl)methylene)amino)-HCID 170099—

반응 단계

A mixture of 5.9 g. of p-aminobenzonitrile and 9.5 g. of p-n-hexylbenzaldehyde in 100 ml. of benzene is treated with 150 mg. of p-toluenesulfonic acid and reacted as described in Example 1. After evaporation, there remain 14.4 g. of a brownish oil which crystallizes with cooling. Purification is carried out by several recrystallizations from isopropanol as described in Example 1. The p-[(p-n-hexylbenzyliden)amino]benzonitrile which is obtained has a melting point of 32.2°-33.0°C. and a clearing point of 64.5°C. UV (ethanol): ε281 = 23500 (shoulder at 310 nm). The nuclear magnetic resonance, mass spectrum, infrared and microanalysis data confirm the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03963313
출처 데이터셋uspto-grants-1976_06
ORD IDord-6204ca42da39428fb78272b03b9c356a
출처 메모uspto-grants-1976_06