Azetidine

Azetidine is a saturated heterocyclic organic compound containing three carbon atoms and one nitrogen atom. It is a liquid at room temperature with a strong odor of ammonia and is strongly basic compared to most secondary amines.

Not to be confused with azatadine.
Azetidine
Names
Preferred IUPAC name
Azetidine[1]
Systematic IUPAC name
Azacyclobutane
Other names
Azetane
Trimethylene imine
1,3-Propylenimine
Identifiers
3D model (JSmol)
102384
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.240
EC Number
  • 207-963-8
986
UNII
Properties
C3H7N
Molar mass 57.09 g/mol
Appearance colorless liquid
Density 0.847 g/cm3 at 25 °C
Boiling point 61 to 62 °C (142 to 144 °F; 334 to 335 K)
miscible
Acidity (pKa) 11.29 (conjugate acid; H2O)[2]
Hazards
Main hazards Somewhat strong base, combustible
GHS pictograms
GHS Signal word Danger
GHS hazard statements
 H225, H314
P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P370+378, P403+235, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Synthesis and occurrence

Azetidines can be prepared by reduction of azetidinones (β-lactams) with lithium aluminium hydride. Even more effective is a mixture of lithium aluminium hydride and aluminium trichloride, a source of "AlClH2" and "AlCl2H".[3] Azetidine can also be produced by a multistep route from 3-amino-1-propanol.[4]

Regio- and diastereoselective synthesis of 2-arylazetidines could be performed from appropriately substituted oxyranes via ring transformation. It is controlled by Baldwin’s Rules with remarkable functional group tolerance.

Azetidine and its derivatives are relatively rare structural motifs in natural products. They are a component of mugineic acids and penaresidins. Perhaps the most abundant azetidine containing natural product is azetidine-2-carboxylic acid, a toxic homolog of proline.[5]

gollark: Of course it is.
gollark: *We*'ve entered the biphasic dopamine phase, thanks to superior memetics.
gollark: We will shortly be entering the gas phase. It is time to leave the π/2 phase behind.
gollark: So is it Macron?
gollark: Well, you won't see with Macron, because it doesn't exist.

See also
  • Azete, the unsaturated analog

References
  1. "Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 147. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  2. Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. p. 5–89. ISBN 978-1498754286.
  3. Alcaide, Benito; Almendros, Pedro; Aragoncillo, Cristina (2007). "Β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products". Chemical Reviews. 107 (11): 4437–4492. doi:10.1021/cr0307300. PMID 17649981.
  4. Donald H. Wadsworth (1973). "Azetidine". Organic Syntheses. 53: 13. doi:10.15227/orgsyn.053.0013.
  5. Kovács, Ervin; Ferenc, Faigl; Zoltan, Mucsi (Aug 10, 2020). "Regio- and Diastereoselective Synthesis of 2-Arylazetidines. Quantum Chemical Explanation of Baldwin's Rules for the Ring-formation Reactions of Oxiranes". Journal of Organic Chemistry. doi:10.1021/acs.joc.0c01310. Retrieved Aug 10, 2020.


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