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HRID 602847作成日:2026年10月26日

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

https://huagongshe.com/reaction/602847

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1-Bromo-4-tert-butylbenzeneHCID 77595—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒HexaneHCID 8058—
生成物1-Methyl-3-(4-t-butylphenyl)-cyclopentadieneHCID 8662957069.3%

反応手順

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%).

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-1f47fe57eb444ffb856be1ac35fc2d0f
出典メモuspto-grants-2011_03