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HRID 1594912作成日:2026年10月25日

Benzyl Bromide → 3-Ethyl-3-(3-benzyloxy-phenyl)-azepan-2-one

https://huagongshe.com/reaction/1594912

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Cesium carbonateHCID 10796—
反応物3-Ethyl-3-(3-hydroxy-phenyl)-azepan-2-oneHCID 21706219—
溶媒DimethylformamideHCID 6228—
生成物3-Ethyl-3-(3-benzyloxy-phenyl)-azepan-2-oneHCID 21706301—

反応手順

To a solution of 3-ethyl-3-(3-hydroxy-phenyl)-azepan-2-one (Example 8, Step B) (1.28 g, 0.0055 mol) in DMF (50 mL) was added Cs2CO3 (1.79 g, 0.055 mmol) and benzyl bromide (0.653 mL, 0.0055 mmol) at ambient temperature. After 1.5 h the reaction was concentrated to remove most of the DMF and the residue was partitioned between EtOAc and H2O. The aqueous layer was washed with EtOAc, the organics combined, washed with brine, and dried (MgSO4). Filtration and concentration to dryness gave the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06284755B1
出典データセットuspto-grants-2001_09
ORD IDord-9661498932954ddb9d7d8ff4445cbc5e
出典メモuspto-grants-2001_09