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HRID 1653917作成日:2026年10月26日

Triethylamine → Ethyl 2-hydroxy-5-[[4-(4-methylphenoxysulfonyl)phenyl]ethynyl]benzoate

https://huagongshe.com/reaction/1653917

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Triethylamine hydroiodideHCID 10889681—
反応物Ethyl 2-hydroxy-5-iodobenzoateHCID 13013012—
反応物4-Methylphenyl 4-ethynylbenzenesulfonateHCID 19423410—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-hydroxy-5-[[4-(4-methylphenoxysulfonyl)phenyl]ethynyl]benzoateHCID 19423388—

反応条件

温度50 °C

反応手順

Ethyl 2-hydroxy-5-iodobenzoate (58.5 g, 0.2 mol), 4-methylphenyl 4-ethynylbenzenesulfonate (54.4 g, 0.2 mol) and triethylamine (40 g, 0.4 mol) were dissolved in tetrahydrofuran (100 g). The solution was heated to 50° C. and dichlorobis(triphenylphosphine)palladium (0.5 g, 0.72 mmol) and copper(I)iodide (1 g, 5.2 mmol) were) added simultaneously with stirring. The reaction mixture turned dark and triethylamine hydroiodide started to precipitate after about 10 min. After keeping at 45° C. for 45 min, the suspension was poured into dilute hydrochloric acid and the mixture was extracted with toluene. The toluene solution was evaporated to dryness. The residue was triturated with acetonitrile, filtered off and dried. Yield 73 g, (84%). The pooled material from several batches (270 g) was recrystallized from acetonitrile (1.2 l). Yield 250 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05403930
出典データセットuspto-grants-1995_04
ORD IDord-27359a37178a4bbab4b2cf9f9c3d5332
出典メモuspto-grants-1995_04