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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602846생성일: 2026년 10월 25일

Hydrochloric Acid → 1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadiene

https://huagongshe.com/reaction/602846

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-MethylcyclopentanoneHCID 14265—
반응물Benzene, 1-bromo-3,5-dimethyl-HCID 136357—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadieneHCID 8662956946%

반응 단계

1-Bromo-3,5-dimethylbenzene (13.6 g, 73.6 mmol) was dissolved in a mixed solution of hexane (150 mL) and diethyl ether (20 mL) and added dropwise at 0° C. with a solution (46.6 mL, 1.58M) of n-butyllithium in hexane. The solution was immediately warmed to room temperature, stirred night and day and added dropwise at −78° C. to a solution of 3-methyl-2-cyclopentanone (7.3 mL, 74 mmol) in diethyl ether (100 mL). The resultant solution was warmed to room temperature immediately after dropwise addition and stirred for 2 hours. After termination of the reaction, the reaction solution was added with dilute hydrochloric acid, stirred at room temperature for 30 minutes and then subjected to layer separation. The organic layer was dried with magnesium sulfate and then had the solvent distilled off under reduced pressure. The crude product was distilled under reduced pressure (125 to 127° C./0.5 mmHg) to obtain 1-methyl-3-(3,5-dimethyl-phenyl)-cyclopentadiene (6.2 g, yield: 46%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906599B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d148eed8c1fb41e79daedb2f1b5153da
출처 메모uspto-grants-2011_03