ChemicalBook--->CAS DataBase List--->754125-43-4

754125-43-4

754125-43-4 Structure

754125-43-4 Structure
IdentificationBack Directory
[Name]

Methyl 3-(cyclopentylamino)propanoate
[CAS]

754125-43-4
[Synonyms]

Methyl 3-(cyclopentylamino)
Methyl 3-(cyclopentylamino)propanoate
[Molecular Formula]

C9H17NO2
[MDL Number]

MFCD10687312
[MOL File]

754125-43-4.mol
[Molecular Weight]

171.237
Chemical PropertiesBack Directory
[Boiling point ]

256.0±23.0 °C(Predicted)
[density ]

1.00±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

9.76±0.20(Predicted)
Safety DataBack Directory
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2922498590
Hazard InformationBack Directory
[Synthesis]

3-AMINO-PROPIONIC ACID METHYL ESTER

4138-35-6

Cyclopentanone

120-92-3

Methyl 3-(cyclopentylamino)propanoate

754125-43-4

Step 2: Synthesis of methyl 3-(cyclopentylamino)propionate; Methyl 3-aminopropionate (9.37 g, 0.09 mol) was dissolved in dichloromethane (DCM, 200 mL), and cyclopentanone (6.43 mL, 0.07 mol), sodium acetate (5.96 g, 0.07 mol), and sodium triacetoxyborohydride (22 g, 0.10 mol) were added in turn . The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, 20% sodium bicarbonate solution (100 mL) and 2M sodium hydroxide solution (50 mL) were added and separated by extraction with dichloromethane/water (DCM/H?O). The organic phases were combined, washed with saturated sodium chloride (NaCl) solution, dried with anhydrous magnesium sulfate (MgSO?), filtered, and the filtrate was concentrated under reduced pressure and then dried under vacuum to obtain the light yellow oily target product methyl 3-(cyclopentylamino)propionate (8.90 g, 55% yield); the molecular ion peak was detected in the positive mode of mass spectrometry (MS) m/z: 172.4.

[References]

[1] Patent: WO2009/40556, 2009, A1. Location in patent: Page/Page column 44; 75
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