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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 422414생성일: 2026년 10월 25일

Iodine → 1-Quinoxalin-2-yl-but-3-yn-1-ol

https://huagongshe.com/reaction/422414

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Propargyl bromideHCID 7842—
반응물Ammonium ChlorideHCID 25517—
반응물Quinoxaline-2-carbaldehydeHCID 594088—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-Quinoxalin-2-yl-but-3-yn-1-olHCID 86630247—

반응 단계

To a mixture of magnesium (229 mg, 9.41 mmol), mercuric chloride (13 mg, 47 μmol) and few crystals of iodine in Et2O (1.5 mL), a solution of propargyl bromide (0.53 mL, 5.88 mmol) in Et2O (4.5 mL) was added slowly in order to maintain a reflux. The reaction mixture was stirred 1 hour and added to a solution of quinoxaline-2-carbaldehyde (500 mg, 3.16 mmol) in THF (2 mL). The resulting reaction mixture was stirred at 0° C. for 30 min, at room temperature for 30 min and was poured onto saturated NH4Cl solution. The aqueous phase was extracted with Et2O. The aqueous phase was washed with water, brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by C18 flash chromatography (H2O/acetonitrile 100:0 to 80:20) to yield 90 mg (0.45 mmol, 14%) of 1-quinoxalin-2-yl-but-3-ynyl-ol as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101637B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-96286cff0c7b408389a3c9e7c903bf84
출처 메모uspto-grants-2012_01