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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363827생성일: 2026년 10월 25일

Isopropanol → 2-Buten-1-ol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-

https://huagongshe.com/reaction/363827

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Trichloroacetic AcidHCID 6421—
반응물2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enalHCID 3017557—
반응물Aluminum tri-iso-propoxideHCID 16685055—
용매AcetoneHCID 180—
용매TolueneHCID 1140—
생성물2-Buten-1-ol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-HCID 11989781%

반응 단계

3.07 g (15 mmol) of Al(O-i-Pr)3 and 30 ml of toluene were fed into a 100 ml four-necked round bottom flask under atmosphere of nitrogen, and stirred at room temperature, and then 28.8 g (150 mmol) of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-al, then 0.25 g (1.5 mmol) of trichloroacetic acid, and further 18.0 g (300 mmol) of isopropyl alcohol were added while stirring at room temperature. Reaction was conducted while fraction containing acetone generated at the solution temperature of 80° to 92° C. was distilled off. After 6 hours, the reaction solution was analyzed by GLC, 81% of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol was obtained (corresponding to 90% selectivity for conversion of the aldehyde as the starting material).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05874649
출처 데이터셋uspto-grants-1999_02
ORD IDord-3c69ea5d177245898c506b4aba8756cd
출처 메모uspto-grants-1999_02