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HRID 2251709作成日:2026年10月25日

2,4-Dichloroaniline → methyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-1,2,4-triazole-3-carboxylate

https://huagongshe.com/reaction/2251709

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DichloroanilineHCID 11123—
反応物Potassium CarbonateHCID 11430—
反応物Sodium NitriteHCID 23668193—
反応物Dimethyl 2-(4-chlorobenzoylamino)malonateHCID 68614697—
溶媒Acetic AcidHCID 176—
溶媒AcetoneHCID 180—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
生成物methyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-1,2,4-triazole-3-carboxylateHCID 1124604630%

反応手順

Part B: To a stirred suspension of 2,4-dichloroaniline (19.44 gram, 0.12 mol) in concentrated HCl (25 mL) and acetic acid (75 mL) at 0° C. is added a solution of NaNO2 (9.0 gram, 0.13 mol) in water (50 mL) and the resulting solution is stirred for 15 minutes. A solution of dimethyl 2-(4-chlorobenzoylamino)malonate (28.55 gram, 0.10 mol) in acetone (200 mL) is slowly added while keeping the temperature below 0° C. A solution of K2CO3 (120 gram) in water (200 mL) is slowly added and the resulting black mixture is stirred for 30 minutes at 0° C. The mixture is extracted three times with EtOAc. The collected organics are washed with water, aqueous NaHCO3 and water, respectively, dried over MgSO4, filtered and concentrated in vacuo. The residue is dissolved in methanol (500 mL) and a solution of sodium (1 gram) in methanol (75 mL) is added. The resulting stirred mixture is allowed to stand overnight at room temperature and cooled in a refrigerator. The formed precipitate is collected by filtration and washed with methanol to give methyl 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-1,2,4-triazole-3-carboxylate (11.4 gram, 30% yield). Melting point: 153-154° C. 1H-NMR (200 MHz, CDCl3): δ 4.07 (s, 3H), 7.28-7.60 (m, 7H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07319110B2
出典データセットuspto-grants-2008_01
ORD IDord-8af2072e2341499eb1abe845c957fefc
出典メモuspto-grants-2008_01