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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602847생성일: 2026년 10월 26일

Hydrochloric Acid → 1-Methyl-3-(4-t-butylphenyl)-cyclopentadiene

https://huagongshe.com/reaction/602847

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-MethylcyclopentanoneHCID 14265—
반응물1-Bromo-4-tert-butylbenzeneHCID 77595—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물1-Methyl-3-(4-t-butylphenyl)-cyclopentadieneHCID 8662957069.3%

반응 단계

1-Bromo-4-t-butylbenzene (18 mL, 104 mmol) was dissolved in diethyl ether (100 mL) and added dropwise at −30° C. with a solution (66 mL, 104 mmol, 1.57 N) of n-butyllithium in hexane. The resultant solution was warmed to room temperature, stirred night and day and added dropwise at −20° C. to a solution of 3-methyl-2-cyclopentanone (10 g, 104 mmol) in diethyl ether (10 mL). Immediately after dropwise addition, the solution was warmed to room temperature and stirred for 3 hours. After termination of the reaction, the reaction solution was added with dilute hydrochloric acid and 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 (105 to 115° C./0.16 mmHg) to obtain 1-methyl-3-(4-t-butylphenyl)-cyclopentadiene (15.3 g, yield: 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906599B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-1f47fe57eb444ffb856be1ac35fc2d0f
출처 메모uspto-grants-2011_03