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IdentificationBack Directory
[CAS]

1205676-44-3
[Molecular Formula]

C8H13NO2.HCl
[MDL Number]

MFCD10703494
[MOL File]

1205676-44-3.mol
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride(1205676-44-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

(1S,3aR,6aS)-Hexahydro-cyclopenta[c]pyrrole-1,2(1H)-dicarboxylic Acid 2-(tert-Butyl) Ester

597569-42-1

(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride

1205676-44-3

(3) Intermediate 2 (700 g, 2.8 mol, 1.0 eq.) was added to a saturated ethanol solution of hydrogen chloride (3.0 L). Heat was refluxed and stirred for 3 h. Stirring was stopped when the reaction was complete. The ethanol solvent was removed by rotary evaporator and the resulting residue was recrystallized from petroleum ether to give 580 g of ethyl (1S,3aR,6aS)-octahydrocyclopenta[c]pyrrole-1-carboxylate hydrochloride as a white solid. The yield was 96.4% and the enantiomeric excess (ee) was 99.7%.

[References]

[1] Patent: CN105601556, 2016, A. Location in patent: Paragraph 0025; 0045
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