Substances

  • META-DOB

      5-BROMO-2,4-DIMETHOXYAMPHETAMINE SYNTHESIS: The reaction of 2,4-dimethoxyamphetamine (2,4-DMA) with elemental bromine proceeded directly to the formation of 5-bromo-2,4-dimethoxyamphetamine which was isolated as the hydrobromide salt with...

  • MEPEA

    3-METHOXY-4-ETHOXYPHENETHYLAMINE SYNTHESIS: A solution of 10.0 g 3-methoxy-4-ethoxybenzaldehyde in 150 mL nitromethane was treated with 1.7 g anhydrous ammonium acetate, and heated on the steam bath...

  • MEM

    2,5-DIMETHOXY-4-ETHOXYAMPHETAMINE SYNTHESIS: A solution of 83 g bourbonal (also called ethyl vanillin, or vanillal, or simply 3-ethoxy-4-hydroxybenzaldehyde) in 500 mL MeOH was treated with a solution...

  • MEE

      4,5-DIETHOXY-2-METHOXYAMPHETAMINE SYNTHESIS: To a solution of 166 g bourbonal in 1 L MeOH there was added a solution of 66 g KOH pellets in 300...

  • MEDA

        3-METHOXY-4,5-ETHYLENEDIOXYAMPHETAMINE SYNTHESIS: To a solution of 50 g 3,4-dihydroxy-5-methoxybenzaldehyde in 100 mL distilled acetone there was added 70 g ethylene bromide and 58 g...

  • ME; METAESCALINE

    3,4-DIMETHOXY-5-ETHOXYPHENETHYLAMINE SYNTHESIS: To a vigorously stirred suspension of 18.6 g of 5-bromobourbonal in 100 mL CH2Cl2 there was added 14.2 g methyl iodide, 1.0 g decyltriethylammonium...

  • MDPR

      N-PROPYL-MDA; 3,4-METHYLENEDIOXY-N-PROPYLAMPHETAMINE SYNTHESIS: A total of 20 mL concentrated HCl was added beneath the surface of 20 mL propylamine, and when the addition was complete,...

  • MDPL

      N-PROPARGYL-MDA; N-PROPYNYL-MDA; 3,4-METHYLENEDIOXY-N-PROPARGYLAMPHETAMINE) SYNTHESIS: A solution of 10.5 g propargylamine hydrochloride in 40 mL MeOH was treated with 2.0 g 3,4-methylenedioxyphenylacetone (see under MDMA for its...

  • MDPH

      a,a-DIMETHYL-3,4-METHYLENEDIOXY- PHENETHYLAMINE; 3,4-METHYLENEDIOXYPHENTERMINE SYNTHESIS: To 150 mL of THF, under an atmosphere of nitrogen, there was added 11.2 g diisopropylamine, and the solution was cooled with...

  • MDPEA

    3,4-METHYLENEDIOXYPHENETHYLAMINE; HOMOPIPERONYLAMINE SYNTHESIS: A suspension of 4.0 g LAH in 300 mL anhydrous Et2O was stirred and heated to a gentle reflux in an inert atmosphere....