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HRID 336603作成日:2026年10月25日

2-Bromoethyl methyl ether → Methyl 2-(2-methoxyethyl)tricyclo[3.3.1.13,7]decane-2-carboxylate

https://huagongshe.com/reaction/336603

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromoethyl methyl etherHCID 80972—
反応物Lithium diisopropylamideHCID 2724682—
反応物Methyl tricyclo[3.3.1.13,7]decane-2-carboxylateHCID 12600018—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-(2-methoxyethyl)tricyclo[3.3.1.13,7]decane-2-carboxylateHCID 89498778—

反応手順

To a solution of EXAMPLE 56A (0.314 g) in tetrahydrofuran (5 mL) was added dropwise lithium diisopropylamide (1.401 mL) at −78° C. The reaction mixture was stirred for 60 minutes and 2-bromoethyl methyl ether (0.562 g) was added. The reaction mixture was slowly warmed up to room temperature, stirred at room temperature overnight, quenched with saturated aqueous NH4Cl solution (2 mL), and extracted with ether. The combined organic layer was dried over Na2SO4, filtered, concentrated and purified by flash chromotography (silica 40 g, 0%-30% ethyl acetate/hexanes).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889675B2
出典データセットuspto-grants-2014_11
ORD IDord-974c7881d77149fd9fb57a810cf7c4c9
出典メモuspto-grants-2014_11