1-Benzyl-3-aminopiperidine

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Products Intro: Product Name:1-Benzyl-3-piperidinamine dihydrochloride
CAS:60407-35-4
Purity:99% Package:100kg;1.6USD|10kg;3.6USD|1kg;6.6USD
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CAS:60407-35-4
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:60407-35-4
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Products Intro: Product Name:1-benzyl-3-aminopiperidine
CAS:60407-35-4
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1-Benzyl-3-aminopiperidine manufacturers

1-Benzyl-3-aminopiperidine Basic information
Product Name:1-Benzyl-3-aminopiperidine
Synonyms:1-BENZYL-3-PIPERIDINAMINE;1-BENZYL-PIPERIDIN-3-YLAMINE;1-BENZYLPIPERIDIN-3-AMINE;1-BENZYL-3-AMINOPIPERIDINE;3-AMINO-1-BENZYLPIPERIDINE;3-AMINO-1-PHENYLMETHYLPIPERIDINE;1-BENZYLPIPERIDINE-3-AMINE;1-benzyl-piperidine-3-ylamine
CAS:60407-35-4
MF:C12H18N2
MW:190.28
EINECS:
Product Categories:pharmacetical;Piperidine
Mol File:60407-35-4.mol
1-Benzyl-3-aminopiperidine Structure
1-Benzyl-3-aminopiperidine Chemical Properties
Boiling point 82°C/0.01mmHg(lit.)
density 1.037±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form powder to lump
pka10.21±0.20(Predicted)
color White to Almost white
CAS DataBase Reference60407-35-4(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-37
HS Code 29333990
MSDS Information
1-Benzyl-3-aminopiperidine Usage And Synthesis
Chemical PropertiesWhite powder
Synthesis
Acetamide, N-[1-(phenylmethyl)-3-piperidinyl]-

60169-74-6

1-Benzyl-3-aminopiperidine

60407-35-4

Step 2: Preparation of 3-amino-1-benzylpiperidine 2.13 g of 3-(N-acetylamino)-1-benzylpiperidine was dissolved in 10 mL of 6 N hydrochloric acid and the reaction was stirred under reflux conditions for 1 hr. After completion of the reaction, the mixture was cooled to room temperature and the pH was adjusted to 9-10 by slow addition of 6 N aqueous ammonia solution.Subsequently, the mixture was extracted four times with chloroform (15 mL each time), the organic phases were combined and dried over anhydrous sodium sulfate. The dried organic phase was concentrated under reduced pressure to give 1.21 g of 3-amino-1-benzylpiperidine in 96.3% yield. The product was characterized by 1H NMR (CDCl3): δ 7.31 (m, 5H), 3.51 (s, 2H), 2.93-2.61 (m, 3H), 2.06 (t, 1H), 1.90-1.52 (m, 4H), 1.20-1.02 (m, 1H) ppm.

References[1] Patent: EP2754655, 2014, A2. Location in patent: Paragraph 0086; 0088
[2] Patent: US2014/256711, 2014, A1. Location in patent: Paragraph 0201; 0203
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