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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15619생성일: 2026년 10월 25일

Propanal → 2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enal

https://huagongshe.com/reaction/15619

반응식

참여 물질

역할이름HCID투입량
반응물PropanalHCID 527—
반응물3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-HCID 98497—
촉매Acetic AcidHCID 176—
촉매Stearic AcidHCID 5281—
촉매PiperidineHCID 8082—
생성물2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enalHCID 301755794.9%

반응 조건

온도100 °C

반응 단계

A 500 mL four-necked flask equipped with a stirrer, a thermometer, a reflux condenser and a dropping funnel was charged with 171 g (0.98 mol) of campholenic aldehyde (purity: 88%), 3.8 g (0.045 mol) of piperidine and 13.1 g (0.046 mol) of stearic acid, and the contents in the flask were stirred while heating at 100° C. Then, 91 g (1.6 mol) of propionaldehyde was gradually dropped into the flask for 6 h, and the resultant mixture was aged for 1 h and then cooled. Thereafter, 3.2 g (0.053 mol) of acetic acid was added to the mixture to remove amines therefrom, thereby separating the mixture into two layers. The thus separated organic layer was washed with water and separated into two layers, thereby obtaining 295 g (0.93 mol) of 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)-but-2-en-1-al (purity as measured by gas chromatography: 60.6%) (yield based on theoretical amount: 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732644B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5d449bcf8e7f4469af6a74da47b5a3ab
출처 메모uspto-grants-2010_06