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HRID 1734962作成日:2026年10月26日

1-Phenylcyclohexanol → 1-Phenylcyclohexene

https://huagongshe.com/reaction/1734962

反応式

関与物質

役割名称HCID仕込み量
反応物1-PhenylcyclohexanolHCID 15319—
反応物Deuterium OxideHCID 24602—
反応物4-BromophenetoleHCID 68523—
反応物4-PropylcyclohexanoneHCID 142482—
溶媒DichloromethaneHCID 6344—
生成物1-PhenylcyclohexeneHCID 13043—

反応手順

4-Propylcyclohexanone is dissolved in a solvent, e.g., dichloromethane, and heated with heavy water (D2O) in the presence of a base to obtain 4-propylcyclohexanone-2,2,6,6-d4, which is then reacted with a Grignard reagent prepared from 1-ethoxy-4-bromobenzene. The resulting d4 -phenylcyclohexanol derivative is dehydrated to obtain a d3 -phenylcyclohexene derivative. The d3 -phenylcyclohexene derivative is catalytically reduced, and the cis-compound is removed to obtain 1-(trans-4-propylcyclohexyl-2,2,6-d3)-4-ethoxybenzene. ##STR60##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05536443
出典データセットuspto-grants-1996_07
ORD IDord-693aac6a46134b7f9e10d39df891da98
出典メモuspto-grants-1996_07