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ChemicalBook >  Product Catalog >  Organic Chemistry >  Spirocyclic Compounds >  2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester

2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester

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2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester Basic information

Product Name:
2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester
Synonyms:
  • 2,8-diazaspiro[3.4]octane-8-carboxylic acid tert-butyl ester
  • 5-Boc-2,5-diaza-spiro[3.4]octane
  • 5-Boc-2,5-diazaspiro[3.4]...
  • tert-butyl 2,5-diazaspiro[3.4]octane-5-carboxylate
  • 2,5-Diazaspiro[3.4]octane-5-carboxylic acid tert-butyl ester oxalate
  • 2,5-Diazaspiro[3.4]octane-5-carboxylic acid tert-butyl ester
  • tert-Butyl 2,8-Diazaspiro[3.4]octane-8-carboxylate hemioxalate
  • TERT-BUTYL 2,8-DIAZASPIRO[3.4]OCTANE-8-CARBOXYLATE
CAS:
1086398-04-0
MF:
C11H20N2O2
MW:
212.29
Mol File:
1086398-04-0.mol
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2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester Chemical Properties

storage temp. 
2-8°C
form 
solid
Appearance
Colorless to light yellow Solid-Liquid Mixture
InChI
1S/C11H20N2O2/c1-10(2,3)15-9(14)13-6-4-5-11(13)7-12-8-11/h12H,4-8H2,1-3H3
InChIKey
XKASCTCECDLMSI-UHFFFAOYSA-N
SMILES
CC(C)(C)OC(=O)N1CCCC12CNC2
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Safety Information

WGK Germany 
WGK 3
HS Code 
2933998090
Storage Class
11 - Combustible Solids
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2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester Usage And Synthesis

Synthesis

2,5-Diazaspiro[3.4]octane-5-carboxylicacid-1,1-dimethylethylester is a heterocyclic organic compound frequently used as a pharmaceutical intermediate. A few examples of 2,5-diazaspiro[3.4]octanes with N-Boc-protected azetidine nitrogen were obtained by condensation of N-Boc-azetidine-3-one with N-benzylbut-3-yn-1-amine elaborated for a streamlined synthesis of C(sp3)-rich N-heterospirocycles via visible-light-mediated Ir-photocatalyzed reactions[1].

References

[1] Flodén, N.J.; Trowbridge, A.; Willcox, D.; Walton, S.M.; Kim, Y.; Gaunt, M.J. Streamlined Synthesis of C-Rich N-Heterospirocycles Enabled by Visible-Light-Mediated Photocatalysis. J. Am. Chem. Soc. 2019, 141, 8426–8430. DOI:10.1021/jacs.9b03372

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