Basic information Safety Supplier Related

cis-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester

Basic information Safety Supplier Related

cis-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester Basic information

Product Name:
cis-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester
Synonyms:
  • cis-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester
  • tert-Butyl 5-oxo-octahydrocyclopenta-[c]pyrrole-2-carboxylate
  • 2-Boc-5-oxo-hexahydrocyclopenta[c]pyrrole
  • (3aR,6aS)-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid 1,1-dimethylethyl ester
  • (3aR,6aS)-5-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester
  • Cyclopenta[c]pyrrole-2(1H)-carboxylic acid, hexahydro-5-oxo-, 1,1-dimethylethyl ester, (3aR,6aS)-rel-
  • cis-tert-Butyl 5-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
  • tert-butyl cis-5-oxo-octahydrocyclopenta[c]pyrrole-2-carboxylate
CAS:
146231-54-1
MF:
C12H19NO3
MW:
225.28
Mol File:
146231-54-1.mol
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cis-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester Chemical Properties

Melting point:
70-71 °C
Boiling point:
325.8±35.0 °C(Predicted)
Density 
1.139±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-0.82±0.20(Predicted)
form 
solid
color 
White to yellow
InChI
InChI=1/C12H19NO3/c1-12(2,3)16-11(15)13-6-8-4-10(14)5-9(8)7-13/h8-9H,4-7H2,1-3H3/t8-,9+
InChIKey
GGNDIMLSSMWKDR-DTORHVGONA-N
SMILES
C(N1C[C@]2([H])CC(C[C@]2([H])C1)=O)(=O)OC(C)(C)C |&1:3,8,r|
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Safety Information

HS Code 
2933998090
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cis-5-Oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylic acid tert-butyl ester Usage And Synthesis

Synthesis

24424-99-5

96896-09-2

146231-54-1

Cis-hexahydrocyclopentadieno[c]pyrrol-5(1H)-one (2.0 g, 16 mmol) was used as starting material and dissolved in dichloromethane (50 mL). Subsequently, di-tert-butyl dicarbonate (5.2 g, 24 mmol), triethylamine (3.2 g, 32 mmol) and 4-dimethylaminopyridine (195 mg, 1.6 mmol) were added to the solution. The reaction mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, it was quenched by adding water (100 mL) and the aqueous and organic phases were separated. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated to give the crude product. The crude product was purified by silica gel column chromatography (eluent ratio of petroleum ether:ethyl acetate=10:1) to finally obtain tert-butyl cis-5-oxooctahydrocyclopenta[c]pyrrole-2(1H)-carboxylate (3.4 g, 94.4% yield).

References

[1] Patent: US2017/112833, 2017, A1. Location in patent: Paragraph 0550-0551

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