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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1694487생성일: 2026년 10월 25일

Dibutyltin dichloride → 5-Bromo-3-(2,2-dimethyl-[1,3]dioxan-5-ylamino)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1694487

반응식

참여 물질

역할이름HCID투입량
반응물Dibutyltin dichlorideHCID 12688—
반응물PhenylsilaneHCID 12752—
반응물2,2-Dimethyl-1,3-dioxan-5-oneHCID 2733141—
반응물Methyl 3-amino-5-bromothiophene-2-carboxylateHCID 20158931—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-Bromo-3-(2,2-dimethyl-[1,3]dioxan-5-ylamino)-thiophene-2-carboxylic acid methyl esterHCID 5779542929.6%

반응 단계

A suspension of 3-amino-5-bromo-thiophene-2-carboxylic acid methyl ester (0.5 g, 2.12 mmol) in dry THF (0.6 mL) was treated with 2,2-dimethyl-[1,3]dioxan-5-one (253 μl, 2.12 mmol), followed by dibutyltin dichloride (32 mg, 0.11 mmol). After 5 min phenyl silane (280 μl, 2.27 mmol) was added and the reaction was stirred at room temperature for 3 days. It was dissolved in ethyl acetate (100 mL), washed with NaHCO3 solution and brine. The organic layer was separated, dried over MgSO4, evaporated and left on vacuum pump overnight. The residue was triturated with hexane-ether (4:1) mixture (2×100 mL). The soluble portion was evaporated and purified by chromatography over silica gel (hexane:ethyl acetate-95:5) yielding pure 5-bromo-3-(2,2-dimethyl-[1,3]dioxan-5-ylamino)-thiophene-2-carboxylic acid methyl ester (220 mg, 29%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158675B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-547256c628f147049250b8bcf4f85f82
출처 메모uspto-grants-2012_04