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HRID 1143作成日:2026年10月23日

Dimethylformamide → 7-(1-Adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene

https://huagongshe.com/ja/reaction/1143

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物3-(Adamantan-1-yl)-6-bromonaphthalen-2-olHCID 14549072—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
生成物7-(1-Adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthaleneHCID 19694681—

反応手順

11.9 g (33.3 mmol) of 7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene, 120 ml of DMF, 5.1 ml (36.6 mmol) of triethylamine and 203 mg of 4-dimethylaminopyridine were introduced successively into a three-necked flask. A solution of 5.52 g (36.6 mmol) of tert-butyldimethylsilyl chloride was added dropwise and the mixture was stirred at room temperature for 12 hours. The reaction medium was poured into water, extracted with ethyl ether, the organic phase decanted, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a silica column eluted with heptane; 12 g (76%) of 7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene of melting point 120°-121° C. were recovered.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723499
出典データセットuspto-grants-1998_03
ORD IDord-a18ffbdb8f6b474a86827045ded0ce46
出典メモuspto-grants-1998_03