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HRID 1389作成日:2026年10月23日

4-Formylbenzoic acid → 4-[3-Oxo-3-(7,8-dihydro-5-(2-thienyl)-8,8-dimethyl-2-naphthalenyl)-1-propenyl)-benzoic acid

https://huagongshe.com/ja/reaction/1389

反応式

関与物質

役割名称HCID仕込み量
反応物4-Formylbenzoic acidHCID 12088—
反応物Sodium HydroxideHCID 14798—
反応物3,4-Dihydro-1-(2-thienyl)-4,4-dimethyl-6-acetylnaphthaleneHCID 22571541—
溶媒MethanolHCID 887—
生成物4-[3-Oxo-3-(7,8-dihydro-5-(2-thienyl)-8,8-dimethyl-2-naphthalenyl)-1-propenyl)-benzoic acidHCID 54528150—

反応手順

To a solution of 62.6 mg (0.222 mmol) 3,4-dihydro-1-(2-thienyl)-4,4-dimethyl-6-acetylnaphthalene (Compound D33) in 4.0 mL of MeOH were added 33.4 mg (0.222 mmol) of 4-carboxy benzaldehyde, and 240.0 mg (6.00 mmol; 2.0 mL of 3M aqueous NaOH). The resulting solution was stirred at room temperature for 12 h, concentrated under reduced pressure, and the residual oil dissolved in EtOAc. The solution was treated with 10% HCl, and the organic layer washed with H2O, and saturated aqueous NaCl, before being dried over Na2 SO4. Removal of the solvents under reduced pressure gave the title compound as a pale green solid after recrystallization from EtOH.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723666
出典データセットuspto-grants-1998_03
ORD IDord-772b5fad62a14312b842257dffc914b5
出典メモuspto-grants-1998_03