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HRID 462936作成日:2026年10月26日

Dimethylformamide → Anthrone

https://huagongshe.com/reaction/462936

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1,4-DioxaneHCID 31275—
反応物ChartreusinHCID 5281394—
反応物ElsamitrucinHCID 5362259—
溶媒Dimethyl SulfoxideHCID 679—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物AnthroneHCID 7018—
生成物ElsamitrucinHCID 5362259—

反応手順

BBM-2478 A and B were obtained as yellowish-orange crystalline solids. Both components of BBM-2478 are distinguishable from chartreusin by thin layer chromatography (TLC) as shown in Table 5. BBM-2478A is readily soluble in dimethyl sulfoxide, dimethylformamide, dioxane and acidic water, slightly soluble in methanol, ethanol and chloroform and insoluble in other organic solvents. Solubility of BBM-2478B is similar to that of BBM-2478A except that BBM-2478B is insoluble in acidic water. BBM-2478 A and B give positive responses with ferric chloride and anthrone reagents. BBM-2478A shows positive reaction to ninhydrin, while BBM-2478B is negative in the same test. Tollen's and Sakaguchi reactions are negative with both components. The physico-chemical properties of BBM-2478A and B are summarized in Table 6. The UV spectra of the two components are similar, showing maxima at 236, 266, 398 and 422 nm in neutral and acidic solutions and at 240, 268 and 435 nm in alkaline solution. These spectra are closely related to that of chartreusin. The IR spectra of BBM-2478 A and B are illustrated in FIGS. 1 and 2, respectively. The proton (PMR) and 13C-NMR (CMR) spectra of BBM-2478A are shown in FIGS. 3 and 4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04518589
出典データセットuspto-grants-1985_05
ORD IDord-645c37a852a14fc88cc2b0e65d7b4f2d
出典メモuspto-grants-1985_05