Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462936Generated: October 25, 2026

Dimethylformamide → Anthrone

https://huagongshe.com/reaction/462936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,4-DioxaneHCID 31275—
ReactantChartreusinHCID 5281394—
ReactantElsamitrucinHCID 5362259—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductAnthroneHCID 7018—
ProductElsamitrucinHCID 5362259—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518589
Source datasetuspto-grants-1985_05
ORD IDord-645c37a852a14fc88cc2b0e65d7b4f2d
Source noteuspto-grants-1985_05