trans-2-Aminocyclpentanol
trans-2-Aminocyclpentanol Basic information
- Product Name:
- trans-2-Aminocyclpentanol
- Synonyms:
-
- Cyclopentanol, trans-2-amino-
- trans-2-Aminocyclpentanol
- Cyclopentanol,2-amino-,(1R,2R)-rel-(9CI)
- Cyclopentanol, 2-amino-, (1R,2R)-rel-
- rac-(1R,2R)-2-Aminocyclopentan-1-ol, trans
- Benzoylchloride,7-(dimethylamino)-
- rel-(1R,2R)-2-aminocyclopentan-1-ol
- CAS:
- 59260-76-3
- MF:
- C5H11NO
- MW:
- 101.15
- Product Categories:
-
- VARIOUSAMINE
- Mol File:
- 59260-76-3.mol
trans-2-Aminocyclpentanol Chemical Properties
- Boiling point:
- 107-108 °C(Press: 17 Torr)
- Density
- 1.084±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 14.93±0.40(Predicted)
- Appearance
- Colorless to light yellow Liquid
trans-2-Aminocyclpentanol Usage And Synthesis
Synthesis
672310-36-0
930-45-0
To a 50 mL autoclave was added 0.900 g (3.82 mmol) of (S,S)-2-benzyloxycarbonylaminocyclopentanol and 0.36 g of 5% palladium-carbon catalyst. Under nitrogen protection, 4.5 mL of degassed methanol was added to the reaction system. The reaction mixture was stirred under 2 MPa hydrogen pressure at 50 °C for 3 hours. Upon completion of the reaction, the palladium-carbon catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated by rotary evaporator to give 0.59 g of crude product. The percentage enantiomeric excess (ee) of the compound was determined to be more than 99%.1H-NMR (200 MHz, CDCl3) δ: 1.2-1.3 (m, 1H), 1.5 (m, 1H), 1.6-1.7 (m, 2H), 1.9-2.0 (m, 2H), 2.3-2.5 (br, 3H), 3.0 (m, 1H), 3.7 ( m, 1H).
References
[1] Patent: EP1398310, 2004, A1. Location in patent: Page 16-17
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