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HRID 358977作成日:2026年10月25日

Pyridine → 2-(4-Methoxybenzoyl)-4,4-diethylisoxazolidine-3,5-dione

https://huagongshe.com/reaction/358977

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物N-Hydroxy-4-methoxybenzamideHCID 221131—
反応物Diethylmalonyl dichlorideHCID 4149059—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Methoxybenzoyl)-4,4-diethylisoxazolidine-3,5-dioneHCID 10017148—

反応手順

A mixture consisting of 1.67 g (0.0107 mol) of 4-methoxybenzohydroxamic acid, mp 158-159° C (dec.)(lit. mp 156-157° C. (dec.), Beilstein Handbook of Organic Chemistry, series H, vol 10, p. 170), 5 ml of pyridine, and 100 ml of methylene chloride was prepared in a 250 ml round bottom flask. The mixture was cooled in an ice bath, and 2.107 g (0.0107 mol) of diethylmalonyl chloride was added dropwise over a 15 minute period with stirring. The reaction mixture was stirred for 2 hours at room temperature after which time all the hydroxamic acid had dissolved. The solution was extracted two times with 50 ml portions of water, three times with 50 ml portions of 5% hydrochloric acid, and two times with 50 ml portions of 5% sodium carbonate. The methylene chloride was dried (MgSO4) and evaporated to dryness under reduced pressure to give 2.19 g (70.4%) of crude 2-(4-methoxybenzoyl)-4,4-diethylisoxazolidine-3,5-dione as a solid residue Recrystallization of the solid from absolute ethanol gave pure 2-(4-methoxybenzoyl)-4,4-diethylisoxazolidine-3,5-dione as a white solid: mp 116-118° C.; IR (Nujol) 1810 (s,C=0), 1750 (s, C=0), 1690 cm-1 (s, C=0); 1H NMR (400 MHz, CDCl3) 7.83 (d, 2H), 6.98 (d, 2H), 3.89 (t, 3H), 1.95 (q, 4H), 1.01 (t, 6H); High resolution MS, calc'd for: C15H17NO5 : 291.1102. Found: 291.1106. Anal Calc'd for: C15H17NO5C, 61.84; H, 5.88; N, 4.81. Found: C, 61.83; H, 5.76; N, 4.76.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04999366
出典データセットuspto-grants-1991_03
ORD IDord-39b81ddcabb54b0daae4496c259fa827
出典メモuspto-grants-1991_03