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1,5-Dioxaspiro[2.4]heptane

Base Information
  • Chemical Name:1,5-Dioxaspiro[2.4]heptane
  • CAS No.:185-61-5
  • Molecular Formula:C5H8O2
  • Molecular Weight:100.117
  • Hs Code.:2932999099
  • Mol file:185-61-5.mol
1,5-Dioxaspiro[2.4]heptane

Synonyms:1,5-Dioxaspiro[2.4]heptane

Suppliers and Price of 1,5-Dioxaspiro[2.4]heptane
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 1,5-DIOXASPIRO[2.4]HEPTANE 95.00%
  • 5MG
  • $ 504.06
Total 13 raw suppliers
Chemical Property of 1,5-Dioxaspiro[2.4]heptane
Chemical Property:
  • Boiling Point:46-48 °C(Press: 14 Torr) 
  • PSA:21.76000 
  • Density:1.15±0.1 g/cm3(Predicted) 
  • LogP:0.17570 
Purity/Quality:

97% *data from raw suppliers

1,5-DIOXASPIRO[2.4]HEPTANE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • General Description 1,5-Dioxaspiro[2.4]heptane is a spirocyclic compound featuring a cyclopropane ring fused to a 1,3-dioxolane ring. It serves as a key structural motif in biologically active natural products and is a versatile intermediate in organic synthesis. 1,5-Dioxaspiro[2.4]heptane can be synthesized from 2,3-dichloroprop-1-ene via lithiation and subsequent cyclization, with potential further functionalization, such as oxidation to lactones, highlighting its utility in synthetic chemistry.
Refernces

Synthesis of substituted 1,5-dioxaspiro[2.4]heptanes from 2,3-dichloroprop-1-ene

10.1002/1522-2675(200210)85:10<3262::AID-HLCA3262>3.0.CO;2-R

The study focuses on the synthesis of substituted 1,5-dioxaspiro[2.4]heptanes using 2,3-dichloroprop-1-ene as the starting material. The key steps involve a 4,4'-di(tert-butyl)biphenyl (DTBB)-catalyzed lithiation of 2,3-dichloroprop-1-ene in the presence of various symmetrically substituted ketones, yielding methylene-substituted diols. These diols are then treated with NaH and I2 to form 1,5-dioxaspiro[2.4]heptanes. The synthesized compounds can be further oxidized to lactones using RuO2 and NaIO4. The study demonstrates a straightforward and efficient method for synthesizing these compounds, which are important structural units in many biologically active natural products and versatile intermediates in organic synthesis.

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