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HRID 398119作成日:2026年10月26日

Sodium Hydroxide → 2-Methyl-2-(4-{2-[5-Methyl-2-(4-Naphthalen-1-ylphenyl)Oxazol-4-yl]Ethoxy}Phenoxy)Propionic Acid

https://huagongshe.com/reaction/398119

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2-Methyl-2-(4-{2-[5-methyl-2-(4-naphthalen-1-ylphenyl)oxazol-4-yl]ethoxy}-phenoxy) propionic acid ethyl esterHCID 12966836—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methyl-2-(4-{2-[5-Methyl-2-(4-Naphthalen-1-ylphenyl)Oxazol-4-yl]Ethoxy}Phenoxy)Propionic AcidHCID 12966838—

反応条件

温度55 °C

反応手順

Under nitrogen, 2-methyl-2-(4- {2-[5-methyl-2-(4-naphthalen-1-ylphenyl)oxazol-4-yl]ethoxy}-phenoxy) propionic acid ethyl ester (0.53 mmol) in ethanol (2.5 mL) and THF (2.5 mL) was treated with 2.0 N NaOH (2.0 mL). The reaction mixture was stirred at 55° C. for 1 hand concentrated in vacuo. The resulting slurry was suspended in ethyl acetate, acidified to pH 1 with 1N HCl, and partitioned. The organic layer was washed with brine, dried (Na2SO4), and concentrated in vacuo to yield of a white solid. Rf=0.25 in 6:4 ethyl acetate:hexanes; 1H NMR (400 MHz, CDCl3) δ7.96 (d, 2H), 7.78-7.70 (m, 3H), 7.41-7.29 (m, 6H), 6.78-6.60 (m, 4H), 4.04 (t, 2H), 2.84 (t, 2H), 2.22 (s, 3H), 1.37 (s, 6H); MS (EI) 508.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610696B2
出典データセットuspto-grants-2003_08
ORD IDord-ac4cfa6ee59e49e9bf9bbb2c61a74a01
出典メモuspto-grants-2003_08