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HRID 29168作成日:2026年10月23日

Cyclohexyl bromide → N-cyclohexyloxyphthalimide

https://huagongshe.com/ja/reaction/29168

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclohexyl bromideHCID 7960—
反応物N-HydroxyphthalimideHCID 10665—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
溶媒DimethylformamideHCID 6228—
生成物N-cyclohexyloxyphthalimideHCID 10467039—

反応条件

温度55 °C

反応手順

N-hydroxylphthalimide (61.3 mmol, 10.0 g) was dissolved in anhydrous DMF (60 mL) under nitrogen. To the stirring solution, DBU (92.0 mmol, 13.75 mL) was injected followed by cyclohexyl bromide (76.6 mmol, 9.43 mL) and the reaction was warmed to 55° C. After stirring for 15 hours, the reaction was warmed to 80° C. for 5 hours, then cooled to room temperature and concentrated to a red oil. The reaction was partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N NaOH, brine and dried over magnesium sulfate. The solvent was removed under vacuum and the crude product was triturated with hexanes providing 2.89 g (19%) of a yellow solid. Rf: 0.7 (2:1 hexanes/ethyl acetate); H1-NMR (CDCl3): δ 7.80 (2H,m), 7.73(2H,m), 4.21 (1H,m), 2.02-1.98 (2H,m), 1.87-1.82 (2H,m), 1.59-1.53 (4H,m), 1.30-1.24 (2H,m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419967B2
出典データセットuspto-grants-2008_09
ORD IDord-16dd12d525704f8bb2157302ec748a15
出典メモuspto-grants-2008_09