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HRID 249161作成日:2026年10月23日

Iminodibenyl → methyl 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylmethyl)benzoate

https://huagongshe.com/ja/reaction/249161

反応式

関与物質

役割名称HCID仕込み量
反応物IminodibenylHCID 10308—
反応物Methyl 3-(chloromethyl)benzoateHCID 3248988—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物methyl 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylmethyl)benzoateHCID 1902480625.6%

反応条件

温度0 °C

反応手順

To a solution of 10,11-dihydro-5H-dibenz[b,f]azepine (2.44 g) in tetrahydrofuran (25 ml) was added potassium tert-butoxide (2.02 g) at 0° C. The mixture was stirred at 0° C. for 15 minutes, and then a solution of methyl 3-(chloromethyl)benzoate (3.57 g) in tetrahydrofuran (15 ml) was added. The mixture was stirred at 25° C. for 1 hour, and then evaporated. The residue was partitioned between ethyl acetate and 0.1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of hexane and ethyl acetate (40:1) to give methyl 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylmethyl)benzoate (1.10 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212320
出典データセットuspto-grants-1993_05
ORD IDord-5a0392a55da541ecb4f9f07138614fca
出典メモuspto-grants-1993_05