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HRID 322957作成日:2026年10月26日

Methanol → Sodium 4-hydroxy-4-(2-methylphenyl)butanoate

https://huagongshe.com/reaction/322957

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium HydroxideHCID 14798—
反応物t-Butyl 4-hydroxy-4-(2-methylphenyl)butanoateHCID 22010446—
溶媒TetrahydrofuranHCID 8028—
生成物Sodium 4-hydroxy-4-(2-methylphenyl)butanoateHCID 23665160—

反応手順

A solution of t-butyl 4-hydroxy-4-(2-methylphenyl)butanoate, thought to be the (R)-enantiomer, (0.5 g) in tetrahydrofuran (3 mL) and methanol (3 mL) is treated with aqueous sodium hydroxide solution (5 N; 0.5 mL) and stirred at ambient temperature for 8 hours. The reaction mixture is concentrated to dryness. The resulting residue is treated with isopropanol (10 mL) and stirred for 30 minutes, and the resulting precipitate is collected and washed with isopropyl ether, to give sodium 4-hydroxy-4-(2-methylphenyl)butanoate, thought to be the (R)-enantiomer, (300 mg) in the form of a white solid, m.p. above 250° C.; 25[α]D=+34° (c=0.01; CH3OH); [NMR(DMSO-d6) (300 MHz):- 1.58-1.75 (m,2H),2.11(m,2H),2.22(s,3H),4.75(m,1H),7.05-7.48 (m.4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211234B1
出典データセットuspto-grants-2001_04
ORD IDord-ced9dd7567274885b3435da95ecb6232
出典メモuspto-grants-2001_04