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HRID 483071作成日:2026年10月26日

1-Bromopentane → 2-n-Pentoxy-5-nonyl benzophenone

https://huagongshe.com/reaction/483071

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromopentaneHCID 8057—
反応物Sodium HydroxideHCID 14798—
反応物Methanone, (2-hydroxy-5-nonylphenyl)phenyl-HCID 93939—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-n-Pentoxy-5-nonyl benzophenoneHCID 5389387382%

反応手順

A solution of 2-hydroxy-5-nonyl benzophenone, 15 g, in 100 mL methylene chloride was mixed with a solution of 9.25 g NaOH in 100 mL water. To this mixture was added 6.9 g n-pentyl bromide and 1.48 g tetra-n-butylammonium bromide. The whole mixture was then vigorously agitated overnight at 40° C. After cooling to room temperature with 50 mL CH2Cl2. The combined methylene chloride layers were concentrated to an oil, which was taken up in 100 mL petroleum ether and washed with 100 mL water. Finally, the organic layer was dried over anhydrous magnesium sulfate and the volatiles removed under vacuum to give 15 g (82% yield) of 2-n-pentoxy-5-nonyl benzophenone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04578250
出典データセットuspto-grants-1986_03
ORD IDord-c311d96f2e954f6182650344fbe57b25
出典メモuspto-grants-1986_03