2-Methylundecanal

Preparation

The first synthesis of 2-methylundecanal was recorded by Georges Darzens in 1904 from methyl nonyl ketone and ethyl chloroacetate. This method of synthesis can be used to produce a variety of aldehydes and became known as the Darzens reaction and is still used today. 2-Methylundecanal is synthesized in industry by two main routes. The first route, like Darzens, involves converting methyl nonyl ketone to its glycidate by allowing it to react with alkyl chloroacetate. The glycidate then undergoes saponification followed by decarboxylation.

:CH3(CH2)8C(O)CH3 + ClCH2CO2R → CH3(CH2)8CH(CH3)OCH(CO2R) + HCl :CH3(CH2)8CCH3OCCO2R + H2O → CH3(CH2)8CH(CH3)CHO + CO2 + ROH

The second method for the synthesis of 2-methylundecanal begins with the conversion of undecanal to 2-methyleneundecanal by allowing it to react with formaldehyde in the presence of base. The 2-methyleneundecanal is then hydrogenated to give 2-methylundecanal. The resulting solution is over 50% 2-methyleneundecanal. The double bond of this compound is hydrogenated and the resulting 2-methylundecanal is separated from the by-products using fractional distillation. The required undecanal in the first step is generated from 1-decene by hydroformylation.

:CH3(CH2)7CH2=CH2 + H2 + CO → CH3(CH2)10CHO :CH3(CH2)10CHO + HCHO → CH3(CH2)8C(CH2)CHO + H2O :CH3(CH2)8C(CH2)CHO + H2 → CH3(CH2)8CH(CH3)CHO

Chirality

2-Methylundecanal contains one asymmetric carbon atom.

The enantiomers can be synthesized with high enantiomeric purity using the SAMP/RAMP hydrazone method. This process involves starting with simple achiral aldehydes and converting them either to their SAMP or RAMP chiral hydrazones using SAMP or RAMP as a chiral auxiliary. The chiral hydrazones are then metalated with lithium diisopropylamide (LDA) and alkylated with a slight excess of dimethyl sulfate. Testing of the enantiomers by a professional perfumer indicated only a slight difference in odor quality and intensity.

Applications

2-Methylundecanal is used widely as a fragrance element in soaps and detergents as well as in the perfume industry to give conifer notes, fir in particular, but is also used in fantasy compositions. This aldehyde was one of the first synthetics to be used in a prestigious perfume, namely Chanel No. 5.

References

References

1. (26 March 2005). "2-Methylundecanal - Compound Summary". National Center for Biotechnology Information.
2. Fenorali, Giovanni. (2004). "Fenorali's Handbook of Flavor Ingredients". CRC Press.
3. [http://www.chm.bris.ac.uk/motm/chanel5/c5jm.htm Molecule of the Month: Chanel No 5 and 2-methylundecanal]
4. (2008–2009). "CRC Handbook of Chemistry and Physics". CRC Press.
5. Darzens, Georges. (1904). "Comptes Rendus Hebdomadaires des séances de l'Académie des Sciences".
6. (2009). "Ullmann's Encyclopedia of Industrial Chemistry". John Wiley & Sons Inc..
7. Dyker, Hubert. (1990). "Synthesis and Properties of Enantiomers of the Two Artificial Fragrances Lilial and Methylundecanal".
8. Ramsden, E.N.. (2000). "A-Level Chemistry". Nelson Thornes.