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HRID 132104作成日:2026年10月27日

Cyclohexanone → 1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanol

https://huagongshe.com/reaction/132104

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanoneHCID 7967—
反応物PentaneHCID 8003—
反応物1-Bromo-3-tert-butylbenzeneHCID 343798—
反応物HCID 178418306HCID 178418306—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Ammonium ChlorideHCID 25517—
生成物1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanolHCID 5973374381%

反応手順

A solution of 1.7 M tert-butyllithium in pentane (32.0 mL, 54.4 mmol) was added to a solution of 1-bromo-3-tert-butyl-benzene (5.54 g, 26.0 mmol) in tetrahydrofuran (60 mL) at −78° C. After stirring for 1 h, cyclohexanone (2.00 g, 18.2 mmol) in tetrahydrofuran (15 mL) was added. After stirring for 18 h, during which time the solution warmed to ambient temperature, the solution was diluted with saturated aqueous ammonium chloride and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was flash chromatographed with 49:1, 24:1, 23:2 hexanes:ethyl acetate as the eluant to yield 3.61 g (81% yield) of 1-(3-tert-butyl-phenyl)-4-methylene-cyclohexanol as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07385085B2
出典データセットuspto-grants-2008_06
ORD IDord-f0668dfcdcd04782a255a587cf61429e
出典メモuspto-grants-2008_06