Réaction #64129
ord-8ac1f04fc7bf4b3182f969b016355951
Équation de réaction
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1ExtractionIt is extracted with dichloromethane
- 2Séchagethe organic phases are dried with sodium sulfate
- 3workup.DISTILLATIONthe solvent is distilled off
- 4AutreThe residue is chromatographed on silica gel with dichloromethane/methanol
- 5Autre406 mg (45% of theory) is isolated
Mode opératoire
838 mg of 3-(2-bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea (2 mmol) is dissolved in 100 ml of dichloromethane, 1.2 g of anhydrous aluminum chloride (9 mmol) and 1.8 ml of dichloromethyl methyl ether (20 mmol) are added and stirred for 15 minutes at room temperature. The reaction mixture is mixed with ice and, after 15 minutes, with a solution of 1.5 g of tartaric acid in 50 ml of water and made alkaline with 5 ml of conc. ammonia solution. It is extracted with dichloromethane, the organic phases are dried with sodium sulfate and the solvent is distilled off. The residue is chromatographed on silica gel with dichloromethane/methanol, 406 mg (45% of theory) is isolated.