Formetorex

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Formetorex
An image of formetamide
Names
Preferred IUPAC name
N-(1-Phenylpropan-2-yl)formamide
Other names
Formetorex
N-Formylamphetamine
N-(alpha-Methylphenethyl)formamide
Identifiers
3D model (
JSmol
)
1563
ChEMBL
ChemSpider
UNII
  • InChI=1S/C10H13NO/c1-9(11-8-12)7-10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3,(H,11,12)
  • CC(CC1=CC=CC=C1)NC=O
Properties
C10H13NO
Molar mass 163.220 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Formetorex (

INN), also known as formetamide or N-formylamphetamine, is a substituted amphetamine described as an anorectic which does not appear to have ever been marketed.[1]

Formetorex is also an

intermediate in the production of amphetamine by the "Leuckart reaction."[2] It is also commonly found as an impurity in clandestine labs where this synthesis method is used.[2][3] Due to the simplicity of the Leuckart reaction, it is the most popular synthetic route employed for the illicit manufacture of amphetamines.[2] The synthesis involves a non-metal reduction that is typically carried out in three steps.[2] For amphetamine synthesis, a mixture of phenylacetone and formamide (sometimes in the presence of formic acid) or ammonium formate, is heated until a condensation reaction results in the intermediate product, formetamide.[2] In the second step, formetamide is hydrolysed using hydrochloric acid, and the reaction mixture is then basified, isolated, and steam distilled to produce the free base.[2] The final step, the product is dissolved in an organic solvent and precipitated as the sulphate salt of amphetamine by adding sulfuric acid.[2]

Diagram of amphetamine synthesis via the Leuckart reaction
Amphetamine synthesis via the Leuckart reaction

References

External links