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HRID 2106764作成日:2026年10月26日

Ethyl Bromide → 3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/2106764

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物Potassium HydroxideHCID 14797—
反応物1-(4-Nitrophenyl)pyrimidine-2,4-dioneHCID 11276338—
溶媒DimethylacetamideHCID 31374—
生成物3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedioneHCID 1512547965.6%

反応手順

A mixture of 3 parts of 1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione, 1,4 parts of potassium hydroxide and 67.5 parts of N,N-dimethylacetamide was stirred for 1 hour at room temperature under nitrogen atmosphere. 1.52 Parts of bromoethane were added and stirring was continued overnight at room temperature. The reaction mixture was poured into 100 parts of ice water. The product was filtered off and stirred in methanol. The product was filtered off and dried in vacuo at 60° C., yielding 2.4 parts (65.6%) of 3-ethyl-1-(4-nitro-phenyl)-2,4(1H,3H)-pyrimidinedione; mp. 182.5° C. (int. 24).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04931444
出典データセットuspto-grants-1990_06
ORD IDord-d072a9a384e947f2a9bfee02dda21a87
出典メモuspto-grants-1990_06