戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 602846作成日:2026年10月27日

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

https://huagongshe.com/reaction/602846

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-MethylcyclopentanoneHCID 14265—
反応物Benzene, 1-bromo-3,5-dimethyl-HCID 136357—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒HexaneHCID 8058—
生成物1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadieneHCID 8662956946%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906599B2
出典データセットuspto-grants-2011_03
ORD IDord-d148eed8c1fb41e79daedb2f1b5153da
出典メモuspto-grants-2011_03