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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270982생성일: 2026년 10월 25일

3-Methyl-2-cyclopenten-1-one → 1-Tert-butyl-3-methylcyclopenta-1,3-diene

https://huagongshe.com/reaction/270982

반응식

참여 물질

역할이름HCID투입량
반응물3-Methyl-2-cyclopenten-1-oneHCID 17691—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178467773HCID 178467773—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물1-Tert-butyl-3-methylcyclopenta-1,3-dieneHCID 1531984423,815.199%

반응 단계

To a solution obtained by adding 350 ml of dehydrated diethyl ether to 450 ml (0.90 mol) of a tert-butylmagnesium chloride/diethyl ether solution (concentration: 2.0 mol/liter), a solution of 43.7 g (0.45 mmol) of 3-methylcyclopentenone in 150 ml of dehydrated diethyl ether was dropwise added in a nitrogen atmosphere at 0° C. with ice cooling, followed by stirring at room temperature for 15 hours. To the reaction solution, a solution of 80.0 g (1.50 mol) of ammonium chloride in 350 ml of water was dropwise added at 0° C. with ice cooling. To the resulting solution, 2500 ml of water was added, followed by stirring. Then, the organic phase was separated and washed with water. To the organic phase, 82 ml of a 10% hydrochloric acid aqueous solution was added at 0° C. with ice cooling, followed by stirring at room temperature for 6 hours. The organic phase was separated from the reaction solution, washed with water, a saturated sodium hydrogencarbonate aqueous solution, water and a saturated saline solution, and then dried over anhydrous magnesium sulfate. The drying agent was filtered, and from the filtrate the solvent was distilled off to obtain a liquid. The liquid was subjected to vacuum distillation (45-47° C./10 mmHg) to obtain 14.6 g of a light yellow liquid. The analyzed values are given below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449533B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-01741cd0d5bb4765823685d2616c17aa
출처 메모uspto-grants-2008_11