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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1653917생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1653917

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Triethylamine hydroiodideHCID 10889681—
반응물Ethyl 2-hydroxy-5-iodobenzoateHCID 13013012—
반응물4-Methylphenyl 4-ethynylbenzenesulfonateHCID 19423410—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-hydroxy-5-[[4-(4-methylphenoxysulfonyl)phenyl]ethynyl]benzoateHCID 19423388—

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온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05403930
출처 데이터셋uspto-grants-1995_04
ORD IDord-27359a37178a4bbab4b2cf9f9c3d5332
출처 메모uspto-grants-1995_04