Basic information Safety Supplier Related

1-Cyclopropylpiperidin-4-one

Basic information Safety Supplier Related

1-Cyclopropylpiperidin-4-one Basic information

Product Name:
1-Cyclopropylpiperidin-4-one
Synonyms:
  • 1-CYCLOPROPYL-PIPERIDIN-4-ONE
  • 1-CYCLOPROPYLTETRAHYDRO-4(1H)-PYRIDINONE
  • 1-CYCLOPROPYL-4-PIPERIDONE
  • 1-Cyclopropyl-4-piperidinone
  • Carbergoline
  • 1-Cyclopropyl-4-oxopiperidine, (4-Oxopiperidin-1-yl)cyclopropane
  • 1-cyclopropy
  • 1-cyclopropyl-2-piperidinone
CAS:
62813-01-8
MF:
C8H13NO
MW:
139.19
EINECS:
1533716-785-6
Mol File:
62813-01-8.mol
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1-Cyclopropylpiperidin-4-one Chemical Properties

Boiling point:
55°/2mm
Density 
1.151±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
8.18±0.20(Predicted)
form 
low melting crystals
color 
Colourless to light yellow
InChI
InChI=1S/C8H13NO/c10-8-3-5-9(6-4-8)7-1-2-7/h7H,1-6H2
InChIKey
DTUJRJIWGWTNFQ-UHFFFAOYSA-N
SMILES
N1(C2CC2)CCC(=O)CC1
CAS DataBase Reference
62813-01-8(CAS DataBase Reference)
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Safety Information

RIDADR 
1993
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2914390090
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1-Cyclopropylpiperidin-4-one Usage And Synthesis

Uses

1-Cyclopropylpiperidin-4-one

Synthesis

49683-17-2

62813-01-8

Step 2: A solution of ethyl 3-[cyclopropyl-(2-ethoxycarbonyl-ethyl)-amino]-propionate (39 mmol) in anhydrous tetrahydrofuran (65 mL) was added slowly and dropwise to a solution of sodium hydride (60% oil dispersion, 58 mmol) in anhydrous tetrahydrofuran (65 mL). Anhydrous ethanol (39 mmol) was then added. The reaction mixture was heated under reflux conditions for 24 hours. Upon completion of the reaction, the reaction solution was neutralized with dilute acetic acid to pH 7 and subsequently partitioned between water and ethyl acetate. The aqueous layer was extracted with ethyl acetate, the organic phases were combined and dried over sodium sulfate. The solvent was removed by concentration under reduced pressure to give 10.2 g of red oily material. This crude product was mixed with 18% w/w hydrochloric acid (130 mL) and heated at reflux for 5 hours. At the end of the reaction, the pH was adjusted to about 12 with sodium hydroxide (about 31 g) and the crude mixture was extracted with ethyl acetate. The organic phases were combined and dried with sodium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was purified by fractional distillation under reduced pressure (20 mbar) and the fractions with a boiling point of 75 °C (20 mbar) were collected to give 3.6 g (67% yield) of the target product 1-cyclopropyl-piperidin-4-one as a colorless oil. Mass spectrometry (MS) analysis showed m/e: 140.0 (MH+, 100%).

References

[1] Patent: US2006/160855, 2006, A1. Location in patent: Page/Page column 14
[2] Patent: WO2005/123716, 2005, A1. Location in patent: Page/Page column 101
[3] Chemical and Pharmaceutical Bulletin, 1980, vol. 28, # 9, p. 2653 - 2657

1-Cyclopropylpiperidin-4-oneSupplier

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