575456-74-5

Basic information

• Product Name: 5,7-Dioxaspiro[2.5]octane-4,8-dione,1-ethyl-2,6,6-trimethyl-,(1R,2R)-rel-(9CI)
• Synonyms: 5,7-Dioxaspiro[2.5]octane-4,8-dione,1-ethyl-2,6,6-trimethyl-,(1R,2R)-rel-(9CI)
• CAS NO: 575456-74-5
• Molecular Formula: C11H16O4
• Molecular Weight: 212.24
• Product Categories: ETHYL
• Mol File: 575456-74-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5,7-Dioxaspiro[2.5]octane-4,8-dione,1-ethyl-2,6,6-trimethyl-,(1R,2R)-rel-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 5,7-Dioxaspiro[2.5]octane-4,8-dione,1-ethyl-2,6,6-trimethyl-,(1R,2R)-rel-(9CI)(575456-74-5)
• EPA Substance Registry System: 5,7-Dioxaspiro[2.5]octane-4,8-dione,1-ethyl-2,6,6-trimethyl-,(1R,2R)-rel-(9CI)(575456-74-5)

Safety Data

• Hazardous Substances Data: 575456-74-5(Hazardous Substances Data)

Upstream product

• 646-04-8 (E)-pent-2-ene 
• 34107-52-3 2,2-dimethyl-5-(phenyl-λ³-iodaneylidene)-1,3-dioxane-4,6-dione 
• 2033-24-1 cycl-isopropylidene malonate 
• 627-20-3 (Z)-pent-2-ene 

Relevant articles and documents

Rhodium(II)-catalyzed inter- and intramolecular cyclopropanations with diazo compounds and phenyliodonium ylides: Synthesis and chiral analysis

Different classes of cyclopropanes derived from Meldrum's acid (=2,2-dimethyl-1,3-dioxane-4,6-dione; 4), dimethyl malonate (5), 2-diazo-3-(silyloxy)but-3-enoate 16, 2-diazo-3,3,3-trifluoropropanoate 18, diazo(triethylsilyl)acetate 24a, and diazo(dimethylphenylsilyl)acetate 24b were prepared via dirhodium(II)-catalyzed intermolecular cyclopropanation of a set of olefins 3 (Schemes 1 and 4-6). The reactions proceeded with either diazo-free phenyliodonium ylides or diazo compounds affording the desired cyclopropane derivatives in either racemic or enantiomer-enriched forms. The intramolecular cyclopropanation, of allyl diazo(triethylsilyl)acetates 28, 30, and 33 were carried out in the presence of the chiral dirhodium(II) catalyst [Rh 2{(S)-nttl)4}] (9) in toluene to afford the corresponding cyclopropane derivatives 29, 31 and 34 with up to 37% ee (Scheme 7). An efficient enantioselective chiral separation method based on enantioselective GC and HPLC was developed. The method provides information about the chemical yields of the cyclopropane derivatives, enantioselectivity, substrate specifity, and catalytic activity of the chiral catalysts used in the inter- and intramolecular cyclopropanation reactions and avoids time-consuming workup procedures.

Rhodium(II)-catalyzed olefin cyclopropanation with the phenyliodonium ylide derived from Meldrum's acid

The phenyliodonium ylide 3a derived from Meldrum's acid reacts with olefins in the presence of Rh(II) carboxylate catalysts to afford cyclopropanes. The reaction is stereospecific. Enantioselectivities of up to 63% have been observed for the cyclopropanation of pent-1-ene. No 1,3-cycloadducts are formed between 3a and polarized olefins such as furan or 2,3-dihydrofuran.