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HRID 1018374作成日:2026年10月26日

Water → 3-{2-[5-(2-Adamantan-1-yl-ethyl)-1-methyl-2-o-tolyl-1H-imidazol-4-yl]-vinyl}-benzoic acid methyl Ester

https://huagongshe.com/reaction/1018374

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Phosphonium, [[3-(methoxycarbonyl)phenyl]methyl]triphenyl-, bromideHCID 10051285—
反応物5-(2-Adamantan-1-yl-ethyl)-1-methyl-2-o-tolyl-1H-imidazole-4-carbaldehydeHCID 18405418—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-{2-[5-(2-Adamantan-1-yl-ethyl)-1-methyl-2-o-tolyl-1H-imidazol-4-yl]-vinyl}-benzoic acid methyl EsterHCID 70160899—

反応手順

Sodium hydride (60% dispersion in oil) (122 mg, 3.05 mmol) was added to an ice cooled suspension of 3-methoxycarbonyl-benzyl-triphenylphosphonium bromide (1.25 g, 2.54 mmol) in THF (5 ml). The yellow suspension was stirred at room temperature for 10 min, cooled to 0° C. and the solution of the product of step b (7686 mg, 2.12 mmol) in THF (5 ml) was added. The suspension was allowed to warm to room temperature and stirred for 72 h. Water (2 ml), then ethyl acetate (40 ml) were added. The organic phase was washed with water (30 ml), brine (30 ml), dried (MgSO4) and the solvent was evaporated. The crude product was purified by flash column chromatography (silica, hexane/ethyl acetate 5:2) to afford the product as 2:1 mixture of trans/cis isomers (778 mg, 74%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479531B1
出典データセットuspto-grants-2002_11
ORD IDord-67e3a5df10fa4d52a1bf856fb10494f4
出典メモuspto-grants-2002_11