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HRID 618479作成日:2026年10月25日

Water → 7-(1-Adamantyl)-6-benzyloxy-2-bromonaphthalene

https://huagongshe.com/reaction/618479

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzyl BromideHCID 7498—
反応物Sodium hydrideHCID 24758—
反応物3-(Adamantan-1-yl)-6-bromonaphthalen-2-olHCID 14549072—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
生成物7-(1-Adamantyl)-6-benzyloxy-2-bromonaphthaleneHCID 22000359—

反応手順

1.26 g (42 mmol) of sodium hydride (80% in oil) and 50 ml of DMF were introduced into a 3-necked flask, a solution of 12.5 g (35 mmol) of 7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene in 100 ml of DMF was added dropwise and stirring was carried out until gas evolution had ceased. 5 ml (42 mmol) of benzyl bromide were then added and stirring was carried out at room temperature for 2 hours. The reaction mixture was poured into water and extracted with ethyl ether and the organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue obtained was taken up in ethanol, heated to reflux, cooled, filtered and dried. 12.5 g (80%) of the expected compound were collected, which compound had a melting point of 150°-1° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05952382
出典データセットuspto-grants-1999_09
ORD IDord-3d5c682f50c74932bc97b777b9476532
出典メモuspto-grants-1999_09