Réaction #54193

Équation de réaction

aluminum chloride

daunomycinone

daunomycinone

→

(+)-carminomycinone

Solvants

oxalic acid

benzene

Conditions de réaction

Traitement

1. 1
   AutreThe reaction gradually turned purple
2. 2
   workup.STIRRINGstirring
3. 3
   workup.ADDITIONthe layers mixed thoroughly until the color
4. 4
   ExtractionThe aqueous phase was extracted once with chloroform (10 ml)
5. 5
   workup.ADDITIONthe chloroform added to the benzene
6. 6
   LavageThe combined organic phases were washed once with water
7. 7
   Séchagedried over anhydrous sodium sulfate
8. 8
   Concentrationconcentrated

Mode opératoire

Natural daunomycinone (14.7 mg) was taken up in anhydrous benzene (100 ml). Sea sand (1 g) was added and the mixture was stirred until all the daunomycinone went into solution. The reaction was stirred under nitrogen and anhydrous aluminum chloride (0.22 g) was added. The reaction gradually turned purple; stirring was continued at room temperature overnight. The reaction was worked up by pouring in aqueous oxalic acid (25 ml., 25%) and the layers mixed thoroughly until the color was discharged. The aqueous phase was extracted once with chloroform (10 ml) and the chloroform added to the benzene. The combined organic phases were washed once with water, dried over anhydrous sodium sulfate and concentrated to give (+)-carminomycinone, Rf = 0.16 (on silica gel, 3% methanol in methylene chloride, v/v). The mass spectrum showed 384 (M+, 45%), 366 (7%), 348 (100%), 341 (3%), 333 (21%), 323 (67%), 305 (19%), 295 (39%, 277 (16%), 249 (8%). The NMR (CDCl3) taken using Fourier-transform spectroscopy gave δ 13.47, 12.96, 12.17 (s, 1H ea); 7.14-7.25 (m, 3H), 2.43 (s, 3H), 2.27 (m, 2H); the vv spectrum showed maxma at 527, 512, 492, 480 and 466 nm.

Source