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HRID 348424作成日:2026年10月27日

Dichloromethane → 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/348424

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium CarbonateHCID 10340—
反応物2-Bromoethyl methyl etherHCID 80972—
反応物HCID 178438045HCID 178438045—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamideHCID 11218717—

反応手順

A mixture of 3-ethyl-4-nitro-1H-pyrazole-5-carboxamide (2.5 kg, 13.6 Mol), sodium carbonate (1.8 Kg, 17.0 Mol) and 2-bromoethyl methyl ether (1.98 kg, 14.2 Mol) in THF (22.5 L) and water (2.5 L) was heated under reflux and stirred for 20 hours. The mixture was cooled to ambient temperature and CH2Cl2 (67.5 L) and water (22.5 L) were added. The resultant organic and aqueous layers were separated. The aqueous phase was extracted with CH2Cl2 (22.5 L) and the combined organic solution was distilled under atmospheric pressure and replaced with ethyl acetate (33 L) to a final volume of 17 L. The cooled mixture was granulated at ambient temperature for 2 hours, filtered and washed with ethyl acetate (2.5 L). This afforded 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide as a white crystalline solid, 2.10 kg, 57%. m.p.=140° C. Found: C, 44.46; H, 5.79; N, 23.01. C9H14N4O4 requires C, 44.63; H, 5.79; N, 23.14%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176311B2
出典データセットuspto-grants-2007_02
ORD IDord-9587e5b62c124a949c3ffcecd7c14af6
出典メモuspto-grants-2007_02