戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1661953作成日:2026年10月25日

Triethylamine → HCID 178493950、化合物

https://huagongshe.com/reaction/1661953

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物3-Methoxy-2-methyl-4-(methylsulfonyl)benzoic acidHCID 14257014—
反応物HCID 178478934HCID 178478934—
溶媒DichloromethaneHCID 6344—
生成物HCID 178493950HCID 17849395025.5%

反応手順

To a stirred mixture of 3-methoxy-2-methyl-4-(methylsulfonyl)benzoic acid (340 mg, 1.39 mmol) and 5-hydroxy-1-methylpyrazole hydrochloride (230 mg) in anhydrous methylene chloride (10 mL) were added DCC (dicyclohexylcarbodiimide) (315 mg) and triethylamine (260 mg) at room temperature, followed by stirring for 2 hours. The reaction mixture was subjected to filtration through Celite, the filtrate was concentrated, and the obtained residue was dissolved in 10 mL of anhydrous acetonitrile. Triethylamine (260 mg) and acetone cyanohydrin in a catalytic amount were added thereto, and the reaction solution was stirred overnight at room temperature. 150 mL of ethyl acetate was added, and the solution was washed once with a 1N hydrochloric acid aqueous solution and washed once with a saturated brine. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate:methanol=9:1) to obtain 5-hydroxy-1-methylpyrazol-4-yl 3-methoxy-2-methyl-4-(methylsulfonyl)phenyl ketone (115 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030498B2
出典データセットuspto-grants-2011_10
ORD IDord-2e5a6270f0fb4e798574cd6eef5cc67d
出典メモuspto-grants-2011_10