돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 462936생성일: 2026년 10월 25일

Dimethylformamide → Anthrone

https://huagongshe.com/reaction/462936

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1,4-DioxaneHCID 31275—
반응물ChartreusinHCID 5281394—
반응물ElsamitrucinHCID 5362259—
용매Dimethyl SulfoxideHCID 679—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물AnthroneHCID 7018—
생성물ElsamitrucinHCID 5362259—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04518589
출처 데이터셋uspto-grants-1985_05
ORD IDord-645c37a852a14fc88cc2b0e65d7b4f2d
출처 메모uspto-grants-1985_05