25444-79-5

Basic information

• Product Name: 3-Hydroxy-3-phenylcyclohexanone
• Synonyms: 3-Hydroxy-3-phenylcyclohexanone
• CAS NO: 25444-79-5
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.24
• Mol File: 25444-79-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 155-155.5 °C
• Boiling Point: 349.9±42.0 °C(Predicted)
• Appearance: /
• Density: 1.170±0.06 g/cm3(Predicted)
• PKA: 13.52±0.20(Predicted)
• CAS DataBase Reference: 3-Hydroxy-3-phenylcyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Hydroxy-3-phenylcyclohexanone(25444-79-5)
• EPA Substance Registry System: 3-Hydroxy-3-phenylcyclohexanone(25444-79-5)

Safety Data

• Hazardous Substances Data: 25444-79-5(Hazardous Substances Data)

Upstream product

• 78-94-4 methyl vinyl ketone 
• 98-86-2 acetophenone 
• 6303-82-8 1-phenylhexane-1,5-dione 
• 1244024-97-2 OC₆H₈(C₆H₅)B(O₂C₂(CH₃)4) 
• 504-02-9 1,3-cylohexanedione 
• 10345-87-6 3-phenylcyclohex-2-enone 
• 4969-01-1 1,4-dioxaspiro[4.5]decan-7-one 
• 591-51-5 phenyllithium 

Downstream Products

• 10345-87-6 3-phenylcyclohex-2-enone 
• 6303-82-8 1-phenylhexane-1,5-dione 

Relevant articles and documents

Phosphine oxide-catalyzed enantioselective intramolecular aldol reaction via regioselective enolization of unsymmetrical diketones with tetrachlorosilane

The phosphine oxide-catalyzed asymmetric intramolecular aldol reactions of diketones were investigated. The combination of tetrachlorosilane and a chiral phosphine oxide catalyst promoted the acetyl-selective enolization of diketones, and the subsequent intramolecular aldol reaction occurred in an enantioselective manner. The introduction of two trimethylsilyl groups at the 4- and 4'-positions in BINAP dioxide catalyst improved the enantioselectivity. This reaction provides an effective synthetic method to access β-tertiary-hydroxy cyclohexanones in high yields and with high enantioselectivity.

Intramolecular aldol condensations: Rate and equilibrium constants

Rate and equilibrium constants have been determined for both the aldol addition and the elimination steps in the intramolecular condensation reactions of 2,5-hexanedione, 2,6-heptanedione, 1-phenyl-1,5-hexanedione, and 5-oxohexanal. The overall thermodynamics are similar for cyclization of 2,5-hexanedione and 2,6-heptanedione; conversion of 2,5-hexanedione to the corresponding enone is actually more favorable, but the cyclization of 2,5-hexanedione is 2400 times slower than that of 2,6-heptanedione. As expected on the basis of intermolecular analogs, the addition step is less favorable and slower for 1-phenyl-1,5-hexanedione, and the addition step for 5-oxohexanal is more favorable though similar in rate to that for heptanedione. Detailed analysis of the kinetics and equilibrium for all of these compounds, as well as 2-(2-oxopropyl)benzaldehyde, in terms of Marcus theory, leads to the same intrinsic barriers for the intramolecular reactions as were seen previously for the intermolecular reactions. This means that rate constants for intramolecular aldol reactions should be predictable from the energetics of the reactions and that the effective molarity can be calculated. Methods for estimating thermodynamic quantities for reactants and products of these reactions have been examined.