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HRID 322877作成日:2026年10月26日

Sodium hydride → ethyl (RS)-4-(2-methoxycarbonyl-5-benzyloxyphenoxy)-4-phenylbutanoate

https://huagongshe.com/reaction/322877

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Methyl 4-(benzyloxy)-2-hydroxybenzoateHCID 225489—
反応物Ethyl 4-chloro-4-phenylbutanoateHCID 12847348—
溶媒DimethylformamideHCID 6228—
生成物ethyl (RS)-4-(2-methoxycarbonyl-5-benzyloxyphenoxy)-4-phenylbutanoateHCID 2320431057.6%

反応手順

A stirred suspension of sodium hydride (340 mg) in dry dimethylformamide (100 mL) is treated portionwise with methyl 4-benzyloxy-2-hydroxybenzoate (2 g). After stirring at ambient temperature for 30 minutes, it is treated with ethyl (RS)-4-chloro-4-phenylbutanoate (1.9 g) in one portion and stirred for 16 hours at ambient temperature, and then for two hours at 80° C. The reaction mixture is then concentrated in vacuo and the residue is partitioned between ethyl acetate (100 mL) and water (100 mL). The organic layer is dried over magnesium sulphate, filtered and concentrated in vacuo. Flash chromatography of the resulting oil, eluting with 5-10% ethyl acetate/cyclohexane, affords ethyl (RS)-4-(2-methoxycarbonyl-5-benzyloxyphenoxy)-4-phenylbutanoate (2 g), in the form of a yellow oil.

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-7554c6594e5140b6b1022816babaec49
出典メモuspto-grants-2001_04