ChemicalBook CAS DataBase List alpha-Amylcinnamaldehyde

alpha-Amylcinnamaldehyde synthesis

5synthesis methods

Product Name:alpha-Amylcinnamaldehyde
CAS Number:122-40-7
Molecular formula:C14H18O
Molecular Weight:202.29

By condensation of n-amyl aldehyde with cinnamic aldehyde. This method of condensation of aromatic aldehydes with aliphatic aldehydes has the maximum yield in α-amylcinnamic aldehyde with little formation of the inferior homologs. The methyl, ethyl and propyl amylcinnamic aldehyde analogs exhibit a characteristic scent.

111-71-7
238 suppliers
$13.50/100ML

100-52-7 Synthesis

100-52-7
973 suppliers
$17.30/2g

122-40-7
360 suppliers
$20.00/25mL

Yield:122-40-7 97%

Reaction Conditions:

with benzoic acid;L-proline in neat (no solvent) at 125; for 1 h;Inert atmosphere;Aldol Condensation;Reagent/catalyst;Time;

Steps:

The aldol condensation was carried out by taking freshly distilled benzaldehyde (15.8 mmol) along with 40 mol% of the amino acid as a catalyst, 40 mol% of benzoic acid as co-catalyst and n-decane as an internal standard in a three-necked round bottom flask. The reaction was carried out under inert atmosphere at a desired temperature to minimize the oxidation of aldehydes used in the reaction. In order to improve the selectivity for the cross-aldol product and maximize atom efficiency of the reaction, 1-alkanaldehydes (7.9 mmol) were added to the reaction mixture under a controlled condition (1130 μl/h) using a syringe pump. The reaction mixture was colled down to room temperature after completion of the reaction (checked by GC). All the reactions were done in triplicate to ensure the reproducibility of the reaction.

References:

Ganga, Venkata Subba Rao;Abdi, Sayed H.R.;Kureshy, Rukhsana I.;Khan, Noor-Ul H.;Bajaj, Hari C. [Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical,2016,vol. 55A,# 8,p. 950 - 955]

111-71-7
238 suppliers
$13.50/100ML

100-52-7 Synthesis

100-52-7
973 suppliers
$17.30/2g