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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15624생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/15624

반응식

참여 물질

역할이름HCID투입량
반응물PropanalHCID 527—
반응물3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-HCID 98497—
촉매Acetic AcidHCID 176—
촉매PiperidineHCID 8082—
생성물2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enalHCID 301755780.6%

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 2.8 g (0.046 mol) of acetic acid, and the contents in the flask were stirred while heating at 100° C. Then, 92 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 279 g (0.79 mol) of 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)-but-2-en-1-al (purity as measured by gas chromatography: 54.7%) (yield based on theoretical amount: 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732644B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6ed8be084f0a4aabb4f5884d78af949f
출처 메모uspto-grants-2010_06