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HRID 54120作成日:2026年10月26日

Sodium Hydroxide → 4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acid

https://huagongshe.com/reaction/54120

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Ethyl 4-(2',3'-dimethoxyphenyl)-3-phenylbutyrateHCID 19961164—
溶媒MethanolHCID 887—
生成物4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acidHCID 12478543100.2%

反応手順

Ethyl 4-(2',3'-dimethoxyphenyl)-3-phenylbutyrate (40.3 g, 123 mmol), from Step 3, was dissolved in 400 mL of methanol and 62 mL of 3M aqueous sodium hydroxide solution was added in one portion. The reaction mixture was stirred at ambient temperature for 18 h. The reaction mixture was concentrated and the residue was partitioned between 300 mL of diethyl ether and 200 mL of water. The layers were separated and the aqueous layer was adjusted to pH 6 with 6M aqueous hydrochloric acid solution and extracted with 3×200 mL of diethyl ether. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, faltered and concentrated in vacuo to give 37 g (100% yield) of the title compound as a colorless oil. The 1H NMR spectrum was identical to the spectrum reported for the product of Step 5 of Method A, Example 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621133
出典データセットuspto-grants-1997_04
ORD IDord-977908a01ff54d448822db6a60e9a34a
出典メモuspto-grants-1997_04