129286-24-4

Basic information

• Product Name: 5-allyl-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-one
• Synonyms: 5-allyl-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-one
• CAS NO: 129286-24-4
• Molecular Weight: 232.279
• Mol File: 129286-24-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-allyl-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-allyl-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-one(129286-24-4)
• EPA Substance Registry System: 5-allyl-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-one(129286-24-4)

Safety Data

• Hazardous Substances Data: 129286-24-4(Hazardous Substances Data)

Upstream product

• 611-71-2 MANDELIC ACID 
• 6337-34-4 2,2-dimethyl-5-phenyl-1,3-dioxolan-4-one 
• 106-95-6 allyl bromide 
• 591-87-7 Allyl acetate 

Downstream Products

• 89358-17-8 2-phenylpent-4-ene-1,2-diol 
• 129388-29-0 (R)-2-Hydroxy-2-phenyl-pent-4-enoic acid ethyl ester 
• 81037-04-9 (2S)-2-hydroxy-2-phenyl-4-pentenoic acid 
• 62696-41-7 (R)-2-Hydroxy-2-phenyl-4-pentenoic Acid 
• 73698-05-2 (S)-2-Hydroxy-2-phenylpentanoic Acid 
• 6249-80-5 1-phenylbut-3-en-1-one 
• 20978-66-9 ethyl 2-hydroxy-2-phenyl-4-pentanoate 
• 495-41-0 1-phenylbut-2-en-1-one 

Relevant articles and documents

Nucleophilic benzoylation using a mandelic acid dioxolanone as a synthetic equivalent of the benzoyl carbanion. Oxidative decarboxylation of α-hydroxyacids

The synthesis of alkyl aryl ketones using a mandelic acid dioxolanone as a synthetic equivalent (Umpolung) of the benzoyl carbanion is reported. The methodology involves alkylation of the mandelic acid dioxolanone, hydrolysis of the dioxolanone moiety in the alkylated products and oxidative decarboxylation of the resulting α-hydroxyacids. The last step is carried out in a catalytic aerobic way using a Co (III) complex in the presence of pivalaldehyde under very mild conditions.

Lipase AKG mediated resolutions of α,α-disubstituted 1,2-diols in organic solvents; remarkably high regio- and enantio-selectivity

Diols 1, which contain adjacent tertiary and primary hydroxy groups, can be selectively mono-acylated at the primary hydroxy group by many lipases in organic solvents. Since the reaction does not take place at the chiral tertiary centre itself, observed enantioselectivities are usually low. Only the combination of one lipase, lipase AKG (Amano, Pseudomonas sp.), with selected substrates gives high enantioselectivities (E 20 to > 200). Also, the solvent and acyl donor employed influences the outcome. On the basis of the results of lipase AKG towards substrates 1 an active site model for this specific lipase has been developed, which can account for the results obtained. Full experimental details on the synthesis of diols 1 and enzymatic preparation of acetates 2 are given. Also, the absolute stereochemistry of the enzymatically prepared diols 1 has been established by independent synthesis from (R)-mandelic acid.

Pig Liver Esterase Catalyzed Hydrolyses of Racemic α-Substituted α-Hydroxy Esters

Pig liver esterase catalyzed hydrolyses of some α-substituted α-hydroxy esters give product acids and recovered esters in 9-94percent enantiomeric excess.The observed enantiomeric selectivity could be rationalized using a recently proposed active site mod