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1-Phenylethylamine

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1-Phenylethylamine[1]
Chemical structure of 1-Phenylethylamine
Names
Preferred IUPAC name
1-Phenylethan-1-amine
Other names
(±)-1-Phenylethylamine
(±)-α-Methylbenzylamine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.009.588 Edit this at Wikidata
KEGG
  • InChI=1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3 checkY
    Key: RQEUFEKYXDPUSK-UHFFFAOYSA-N checkY
  • InChI=1/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3
    Key: RQEUFEKYXDPUSK-UHFFFAOYAS
  • NC(c1ccccc1)C
  • CC(c1ccccc1)N
Properties
C8H11N
Molar mass 121.183 g·mol−1
Density 0.94 g/mL
Melting point -65 C[citation needed]
Boiling point 187 °C (369 °F; 460 K)
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Corrosive
Related compounds
Related stereoisomers
(R)-(+)- (CAS [3886-69-9])
(S)-(–)- (CAS [2627-86-3])
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

1-Phenylethylamine is the organic compound with the formula C6H5CH(NH2)CH3. Classified as a monoamine, this colorless liquid is often used in chiral resolutions. Like benzylamine, it is highly basic and forms stable ammonium salts and imines.

This compound may be prepared by the reductive amination of acetophenone under various standard conditions for this type of reaction. One major route for this chemical uses the Mignonac reaction, a one-pot protocol using hydrogen gas as the reducing agent:[2]

Reductive amination acetophenone ammonia

The Leuckart reaction, using ammonium formate, is another method for this transformation.[3][4]

See also

References

  1. ^ 1-Phenylethylamine - PubChem Public Chemical Database
  2. ^ John C. Robinson, Jr. and H. R. Snyder (1955). "α-Phenylethylamine". Organic Syntheses; Collected Volumes, vol. 3, p. 717.
  3. ^ Mann, F. G.; Saunders, B. C. (1960). Practical Organic Chemistry, 4th Ed. London: Longman. pp. 223–224. ISBN 9780582444072.
  4. ^ A. W. Ingersoll (1937). "α-Phenylethylamine". Organic Syntheses; Collected Volumes, vol. 17, p. 76.