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HRID 1857318作成日:2026年10月26日

Acetone Cyanohydrin → HCID 178428868、化合物

https://huagongshe.com/reaction/1857318

反応式

関与物質

役割名称HCID仕込み量
反応物Acetone CyanohydrinHCID 6406—
反応物TriethylamineHCID 8471—
反応物3-(4,5-Dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl chlorideHCID 11255083—
反応物HCID 178478934HCID 178478934—
溶媒ChloroformHCID 6212—
生成物HCID 178428868HCID 17842886869.5%

反応手順

To 2.75 g of 3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoic acid were added 30 ml of benzene, then 1.7 ml of thionyl chloride and a drop of pyridine to heat at reflux for 3 hours. The reaction solution was cooled down. The solvent was distilled out under reduced pressure to give 2.90 g of 3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl chloride. Separately 0.93 g of 5-hydroxy-1-methylpyrazole hydrochloride was dissolved in 20 ml of chloroform, and 1.60 g of triethylamine was added, while cooling with ice. Into the obtained solution was added dropwise 10 ml of a chloroform solution containing 1.90 g of 3-(4,5-dihydroisoxazol-3-yl)-4-methylsulfonyl-2-methylbenzoyl chloride to stir at room temperature for 30 minutes, and 0. 76 g of triethylamine and 0.16 g of acetone cyanohydrin were added to further stir overnight. The reaction solution was washed with dilute hydrochloric acid, then with a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was distilled out under reduced pressure. Methanol was added to the residue. The obtained crystals were separated by filtration to give 1.59 g of the title compound as white crystals. m.p. 224~226° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06147031
出典データセットuspto-grants-2000_11
ORD IDord-1147b474f3c24677b77a1a1baeb1d4c4
出典メモuspto-grants-2000_11