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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 902197생성일: 2026년 10월 25일

Acetonitrile → HCID 178482579, 화합물

https://huagongshe.com/reaction/902197

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물3,3-DiphenylacroleinHCID 71027—
반응물9-AminominocyclineHCID 54676112—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물HCID 178482579HCID 17848257997.1%

반응 단계

9-aminominocycline sulfate salt (0.500 g, 0.748 mmol) is dissolved in anhydrous DMF and treated with β-phenylcinnamaldehyde (0.779 g, 3.74 mmol, 5 equivalents) The solution is then treated with DDQ (0.085 g, 0.374 mmol, 0.5 equivalents) and stirred at room temperature for 5 min. ES+ mass spectrometry showed a 1:1 ratio of product and starting material. A second portion of DDQ (0.068 g, 0.300 mmol, 0.4 equivalents) is added. After approximately 5 minutes, acetonitrile (7.5 mL) is added, and the entire reaction mixture is poured slowly into ether (750 mL.) The pink solid is removed by filtration and washed with fresh ether to yield 0.480 g of the crude product. This material is dissolved in water (75 mL) to give a solution at pH 2.2, which is extracted with dichloromethane (2×100 mL.) The pH of the aqueous layer is raised to 3.0 with aqueous ammonia, and the solution is again extracted with dichloromethane (2×100 mL.) The four organic extracts are dried (Na2SO4), filtered and concentrated to a volume of about 2 mL. A small portion of methanol (1 mL) is added, and the concentrated solution is treated dropwise with 1M HCl in ether. The solid precipitate is filtered, washed with fresh ether and dried under vacuum the product as its HCl salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07365087B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-7db64fe582f040dfbc10e4ea06ba3808
출처 메모uspto-grants-2008_04