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HRID 1075962作成日:2026年10月26日

Imidazole, 5-(2-chloroethyl)-1-methyl-2-nitro- → 1-ME-2-NO2-5-Vinyl imidazole

https://huagongshe.com/reaction/1075962

反応式

関与物質

役割名称HCID仕込み量
反応物Imidazole, 5-(2-chloroethyl)-1-methyl-2-nitro-HCID 90183—
反応物Potassium tert-butoxideHCID 23665647—
溶媒BenzeneHCID 241—
生成物1-ME-2-NO2-5-Vinyl imidazoleHCID 93215—

反応手順

To a solution of 18.9 g. of 5-(2-chloroethyl)-1-methyl-2-nitroimidazole (prepared according to the procedure of British Pat. No. 1,222,486) in 2.8 liters of anhydrous benzene cooled to 5°-10° C., 16.8 g. of potassium tert-butoxide is added. Stirring is continued for 2 hours at 5°-10° C. After filtration and concentration to dryness under vacuum at a temperature lower than 50° C., the resulting yellow oily residue is washed three times with 50 ml. of ethyl ether (or light petroleum). The title product is obtained, which is dried under vacuum at 40° C.; yield 12 g. (77.7%). A sample crystallized from ethyl ether melts at 106°-108° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03954789
出典データセットuspto-grants-1976_05
ORD IDord-1dc4c2dcbd484499bf4d0d95e7d51419
出典メモuspto-grants-1976_05