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HRID 277550作成日:2026年10月26日

(Methoxycarbonylsulfamoyl)triethylammonium hydroxide → Ethyl 4-[(7,8-dihydro-8,8-dimethylnaphth-2-yl)ethynyl]benzoate

https://huagongshe.com/reaction/277550

反応式

関与物質

役割名称HCID仕込み量
反応物(Methoxycarbonylsulfamoyl)triethylammonium hydroxideHCID 11032497—
反応物Ethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethylnaphth-2-yl)ethynyl]benzoateHCID 15391671—
溶媒BenzeneHCID 241—
生成物Ethyl 4-[(7,8-dihydro-8,8-dimethylnaphth-2-yl)ethynyl]benzoateHCID 18314555—

反応条件

温度50 °C

反応手順

To a solution of 0.13 g (0.38 mmol) of ethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethylnaphth-2-yl)ethynyl]benzoate (Compound 9) in 15 ml of dry benzene was added 0.67 g (2.90 mmol) of (methoxycarbonylsulfamoyl) triethylammonium hydroxide (Burgess Reagent). The resulting mixture was heated at 50° C. for 30 minutes, cooled to room temperature, partitioned between water (10 ml) and EtOAc (20 ml) and the layers separated. The organic layer was dried over Na2SO4, concentrated in vacuo and purified by flash chromatography (silica, 10% EtOAc-hexane) to yield the title compound as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355806B1
出典データセットuspto-grants-2002_03
ORD IDord-18d88345c7dd4dc19ee35703fceb65f7
出典メモuspto-grants-2002_03