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HRID 16575作成日:2026年10月26日

Bis(2-bromoethyl) ether → Tert-butyl 4-cyanooxane-4-carboxylate

https://huagongshe.com/reaction/16575

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-bromoethyl) etherHCID 21521—
反応物Sodium hydrideHCID 24758—
反応物tert-Butyl cyanoacetateHCID 70693—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-cyanooxane-4-carboxylateHCID 2313161057%

反応手順

To a stirred suspension of NaH (17.7 g, 0.443 mol) in DMF (200 mL) was added dropwise tert-butyl cyanoacetate (25.0 g, 0.177 mol) in DMF (100 mL) at 0° C. under N2. The mixture was allowed to warm to ambient temperature, and stirred for 1 hour. Then, bis(2-bromoethyl)ether (49.3 g, 0.177 mol) was added to the mixture, and the resulting mixture was stirred at 90° C. for 24 h. After cooling to 0° C., the mixture was quenched with water (100 mL). The volatile components were removed by evaporation and the residue was precipitated with a mixture of EtOAc-Toluene (1:2, 500 mL) and water (500 mL). The organic phase was washed with water (500 mL) for three times, dried over Na2SO4, filtered and evaporated. The solid was washed with Hexane and dried in vacuo to give 19.0 g (57%) of the title compound as a white crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737163B2
出典データセットuspto-grants-2010_06
ORD IDord-f69d8475eee74539846885ab791bd680
出典メモuspto-grants-2010_06