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| | (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride Basic information |
| Product Name: | (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride | | Synonyms: | (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride;(1S,3AR,6AS)-OCTAHYDROCYCLOPENTA[C]PYRROLE-1-CARBOXYLIC ACID HCL;Cyclopenta [C] pyrrole-1-carboxylic acid, octahydro - chloride;(3S,3aS,6aR)-1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrole-3-carboxylic acid hydrochloride | | CAS: | 1205676-44-3 | | MF: | C8H13NO2.HCl | | MW: | 191.65526 | | EINECS: | | | Product Categories: | | | Mol File: | 1205676-44-3.mol | ![(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride Structure](CAS/GIF/1205676-44-3.gif) |
| | (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride Chemical Properties |
| storage temp. | Inert atmosphere,Room Temperature |
| | (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride Usage And Synthesis |
| Synthesis | (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 |
| | (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride Preparation Products And Raw materials |
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