Our chemistry

Wide range of industrially scalable reactions

Our facilities and the accumulated experience in the synthesis of organic components give us allow us to offer our customers a wide range of industrially scalable reactions.

Generic organic synthesis processSpecific type process
AcetylationAcetylchloride, acetic anhydride
AcylationO-Acylation, N-Acylation, Sulfonylation, Friedel-Crafts Acylation.
Acid Chloride HandlingAcetyl Chloride.
Aldo CondensationBenzaldehyde
AlkylationN-Alkylation, O-Alkylation, S-Alkylation, Eschweilwer-Clarke react.
AminationDelépine reaction, Reductive Amination.
Aromatic SubstitutionAromatic halogenation.
BrominationBromine.
CarbamoylationCarbon dioxide.
CarboxylationChlorosulfonic acid.
ChloromethylationChlorine gas, Phosphorous Oxychloride etc.
ChlorosulfonationChlorosulfonic acid.
ChlorinationHantsch 1,4 Dihydropyridines Synthesis, Fischer indole synthesis.
EtherificationAlkoxide or Aroxide and Alkyl Halide.
EsterificationAlcohol and Carboxylic Acid.
EliminationDehydration, Aromatization.
Diels-Alder reactionMaleic anhydre.
Delepine ReactionHexamethylene tetramine.
DehydrationSulfuric Acid, Double-bond formation.
DecarboxylationSulfuric Acid.
CyclizationChlorine gas, Phosphorous Oxychloride etc.
Freidel Crafts reactionsAluminium Trichloride.
FormylationPhosphorous Oxychloride
HalogenationAromatic and Aliphatic Bromination and Chlorinations Acyl Halide formations.
Heterocyclic Ring ClosureHantsch 1,4 Dihydropyridines Synthesis, Fischer Indole synthesis.
HydrogenationHydrogen, Catalyst, Rreductive. Amination. Ethylamine.
HydrolysisEster hydrolisis, Amide hydrolisis.
IodinationIodine, Sodium Iodine.
Leuckart reactionAmmonium formate.
Mannich ReactionParaformaldehyde.
Metal Hydride ReductionsSodium Aluminium Hydride, Sodium Borohydride.
NitrationNitric Acid and Sulphuric Acid Mixture.
Nitrogen HeterocyclicsIndoles, Pyridines, 1,4-Dihydropyridines.
OxidationAromatization, Dehydrogenation.
Phase Transfer CatalysisBenzyl Triethylammonium chloride.
Pirrole ChemistryHeterocyclic Substitution.
RearrangementBaker-Ventakaraman rearrangement, Fries rearrangement Schleyer adamantization
ReductionAcetylchloride, acetic anhydride
Reductive aminationKetones and Aldehydes.
TransesterificationMethyl Esters and Higher Alcohols.
SaponificationSodium Hydroxide.
Sulfur ChemistryThiol formation. Sulfoxide Formation.
Vilsmeier-Haack AcylationPhosphorous oxychloride.
Wittig ReactionTriphenylphosphine.