Benzoin
Names
Preferred IUPAC name
2-Hydroxy-1,2-diphenylethan-1-one
Other names
2-Hydroxy-2-phenylacetophenone
2-Hydroxy-1,2-diphenylethanone
Desyl alcohol
Bitter almond oil camphor
Identifiers
3D model (JSmol)
3DMet
391839
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.938 Edit this at Wikidata
KEGG
RTECS number
  • DI1590000
UNII
  • InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H checkY
    Key: ISAOCJYIOMOJEB-UHFFFAOYSA-N checkY
  • InChI=1/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H
    Key: ISAOCJYIOMOJEB-UHFFFAOYAO
  • O=C(c1ccccc1)C(O)c2ccccc2
  • c1ccc(cc1)C(C(=O)c2ccccc2)O
Properties
C14H12O2
Molar mass 212.248 g·mol−1
Appearance Off-white crystals
Density 1.310 g/cm3 (20 °C)[1]
Melting point 135 to 139[1] °C (275 to 282 °F; 408 to 412 K)
Boiling point 330 to 356[1] °C (626 to 673 °F; 603 to 629 K)
Slightly soluble
Solubility in ethanol Very good[1]
Solubility in ether Slightly soluble
Solubility in chlorine Soluble
Solubility in chloroform Very good[1]
Hazards
GHS labelling:
H412
P273, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
1
0
Lethal dose or concentration (LD, LC):
10.000 mg/kg
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 ?)

Benzoin (/ˈbɛnzoʊ.ɪn/ or /-ɔɪn/) is an organic compound with the formula PhCH(OH)C(O)Ph. It is a hydroxy ketone attached to two phenyl groups. It appears as off-white crystals, with a light camphor-like odor. Benzoin is synthesized from benzaldehyde in the benzoin condensation. It is chiral and it exists as a pair of enantiomers: (R)-benzoin and (S)-benzoin.

Benzoin is not a constituent of benzoin resin obtained from the benzoin tree (Styrax) or tincture of benzoin. The main component in these natural products is benzoic acid.

History

Benzoin was first reported in 1832 by Justus von Liebig and Friedrich Woehler during their research on oil of bitter almond, which is benzaldehyde with traces of hydrocyanic acid.[2] The catalytic synthesis by the benzoin condensation was improved by Nikolay Zinin during his time with Liebig.[3][4]

Uses

The main use of benzoin is as a precursor to benzil, which is used as a photoinitiator.[5][6] The conversion proceeds by organic oxidation using copper(II),[7] nitric acid, or oxone. In one study, this reaction is carried out with atmospheric oxygen and basic alumina in dichloromethane.[8]

Benzoin also sees wide spread use in powder coating formulations, where it acts as a degassing agent during the curing stage. This action prevents surface defects such as 'pinholing'.[9][10]

Benzoin can be used in the preparation of several pharmaceutical drugs including oxaprozin, ditazole, and phenytoin.[11]

Preparation

Benzoin is prepared from benzaldehyde via the benzoin condensation.[12]

References

  1. ^ a b c d e William M. Haynes (2016). CRC Handbook of Chemistry and Physics (97th ed.). Boca Raton: CRC Press. p. 3-40. ISBN 978-1-4987-5429-3.
  2. ^ Wöhler, Liebig; Liebig (1832). "Untersuchungen über das Radikal der Benzoesäure". Annalen der Pharmacie. 3 (3): 249–282. doi:10.1002/jlac.18320030302. hdl:2027/hvd.hxdg3f.
  3. ^ N. Zinin (1839). "Beiträge zur Kenntniss einiger Verbindungen aus der Benzoylreihe". Annalen der Pharmacie. 31 (3): 329–332. doi:10.1002/jlac.18390310312. Archived from the original on 2022-07-09. Retrieved 2020-09-10.
  4. ^ N. Zinin (1840). "Ueber einige Zersetzungsprodukte des Bittermandelöls". Annalen der Pharmacie. 34 (2): 186–192. doi:10.1002/jlac.18400340205. Archived from the original on 2022-07-09. Retrieved 2019-06-30.
  5. ^ Hardo Siegel, Manfred Eggersdorfer "Ketones" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, 2002 by Wiley-VCH, Wienheim. doi:10.1002/14356007.a15_077
  6. ^ Nakamura, Kenichiro (2015). Photopolymers : photoresist materials, processes, and applications. Boca Raton, FL. ISBN 978-1-4665-1731-8. OCLC 884012539.((cite book)): CS1 maint: location missing publisher (link)
  7. ^ Clarke, H. T.; Dreger.E. E. (1941). "Benzil". Organic Syntheses; Collected Volumes, vol. 1, p. 87.
  8. ^ Konstantinos Skobridis; Vassiliki Theodorou; Edwin Weber (2006). "A very simple and chemoselective air oxidation of benzoins to benzils using alumina". Arkivoc. 06-1798JP: 102–106.[permanent dead link]
  9. ^ Maxwell, B.E; Wilson, R.C; Taylor, H.A; Williams, D.E; Farnham, W; Tria, J (November 2001). "Understanding benzoin's mode of action in powder coatings". Progress in Organic Coatings. 43 (1–3): 158–166. doi:10.1016/S0300-9440(01)00181-3.
  10. ^ Jahromi, Shahab; Mostert, Ben; Derks, Andreas; Koldijk, Fokelien (December 2003). "Mechanism of action of benzoin as a degassing agent in powder coatings". Progress in Organic Coatings. 48 (2–4): 183–193. doi:10.1016/S0300-9440(03)00096-1.
  11. ^ U.S. patent 2,242,775
  12. ^ Roger Adams; C. S. Marvel (1921). "Benzoin". Organic Syntheses. 1: 33; Collected Volumes, vol. 1, 1941, p. 94.

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