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HRID 344734作成日:2026年10月25日

4-Methyl-2-nitrophenol → Ethyl 2-methyl-2-(4-methyl-2-nitrophenoxy)propanoate

https://huagongshe.com/reaction/344734

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-2-nitrophenolHCID 8391—
反応物Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
反応物Sodium HydroxideHCID 14798—
反応物Sodium hydrideHCID 24758—
溶媒Ethyl AcetateHCID 8857—
溶媒2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
生成物Ethyl 2-methyl-2-(4-methyl-2-nitrophenoxy)propanoateHCID 450746224.9%

反応手順

A solution of 2-nitro-4-methylphenol (11.48 g) in 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) (50 ml) was cooled at 5° C. and treated with portions of sodium hydride (55% w/w dispersion in mineral oil, 3.27 g). The mixture was stirred at room temperature for 2 hours, then cooled to 5° C. and treated with ethyl 2-bromo-2-methylpropionate (13.15 g). The mixture was heated at about 100° C. for 18 hours, then cooled to room temperature and poured into a mixture of aqueous sodium hydroxide solution (1M) and ethyl acetate. The organic solution was separated and washed twice with 1M sodium hydroxide solution, then dried (MgSO4) and concentrated. The resulting oil was purified by flash column chromatography, eluting with a mixture of ethyl acetate and hexane, (increasing from 5:95 v/v to 10:90 v/v), to give ethyl 2-methyl-2-(2-nitro-4-methylphenoxy)propionate (4.48 g) as an oil; NMR: 1.25 (3H, t), 1.60(6H, s), 2.35(3H, s), 4.25(2H, q) and 6.8-7.6(3H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05053415
出典データセットuspto-grants-1991_10
ORD IDord-45dd9e86968a45b98eddc8fc4b0e86f0
出典メモuspto-grants-1991_10