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BENPROPERINE

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BENPROPERINE Basic information

Product Name:
BENPROPERINE
Synonyms:
  • BENPROPERINE
  • 1-(1-methyl-2-((alpha-phenyl-o-tolyl)oxy)ethyl)-piperidin
  • 1-(1-methyl-2-((alpha-phenyl-o-tolyl)oxy)ethyl)piperidine
  • 1-(1-methyl-2-(2-(phenylmethyl)phenoxy)ethyl)-piperidin
  • 1-(2-(2-benzilfenossi)-1-metiletil)-piperidina
  • pirexyl
  • Benproperin
  • 1-[2-(2-Benzylphenoxy)-1-methylethyl]piperidine
CAS:
2156-27-6
MF:
C21H27NO
MW:
309.45
EINECS:
1308068-626-2
Mol File:
2156-27-6.mol
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BENPROPERINE Chemical Properties

Boiling point:
bp0.2 159-161°
Density 
1.0350 (rough estimate)
refractive index 
1.5614 (estimate)
solubility 
DMSO:1.0(Max Conc. mg/mL);3.23(Max Conc. mM)
PBS (pH:7.2):1.0(Max Conc. mg/mL);3.23(Max Conc. mM)
pka
9.46±0.50(Predicted)
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Safety Information

Toxicity
LD50 orally in mice: 1087 mg/kg (Tellini, De Fina)
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BENPROPERINE Usage And Synthesis

Originator

Tussafug,Medipharm,Switz.

Definition

ChEBI: 1-[1-[2-(phenylmethyl)phenoxy]propan-2-yl]piperidine is a diarylmethane.

Manufacturing Process

A mixture of 26.1 g of o-benzylphenoxy-β-chloropropane and 17 g of piperidine is refluxed over a period of 32 hours until the temperature is about 124°C and a nearly solid mixture is formed due to the precipitation of a salt. The mixture is then refluxed over a period of 48 hours at about 160°C and the reaction product obtained is cooled and dissolved in methanol. The solution is concentrated under reduced pressure to yield an oil which is added to 200 ml 3N hydrochloric acid whereupon the mixture is shaken with ether, 3 x 100 ml, until the aqueous phase is clear. The ether solution is washed with water, 3 x 50 ml, and the water present in the combined aqueous phase and water used for washing is evaporated under reduced pressure methanol being added three times when the residue appears to be dry. The impure hydrochloride of o-benzylphenoxy-β-N-piperidinopropane, 41 g, obtained is dissolved in 100 ml water and 100 ml 30% aqueous sodium hydroxide solution are added, whereupon precipitated oil is extracted with ether, 1 x 100 and 2 x 50 ml. The ether solution is washed with water, 4 x 50 ml, dried with magnesium sulfate and the ether is removed under reduced pressure. The residue, 25.2 g, is distilled under reduced pressure and the main fraction, 23.2 g, BP 159°-161°C/0.2 mm.

Therapeutic Function

Antitussive

BENPROPERINE Preparation Products And Raw materials

Raw materials

BENPROPERINESupplier

Wuhan Fortuna Chemical Co., Ltd
Tel
027-59207852 13308628970
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buy@fortunachem.com
Shenzhen SUNGENING Bio-Medical Co., Ltd.
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0755-28967200 13631290199
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wxf@sungening.com
JinJin Le Chemical Co., Ltd
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10106090
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jjlchem2@163.com
Hubei Xinyuanshun Pharmaceutical Chemical Co., Ltd.
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027-51831887 15337167856
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hubeixinyuanshun@163.com
Chengdu Saint - Kay Biotechnology Co., Ltd.
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028-85157043 15882256948
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676046971@qq.com