4-(2-METHOXYPHENYL)PIPERIDINE

4-(2-METHOXYPHENYL)PIPERIDINE Suppliers list
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718; +8613336195806
Email: sales@capot.com
Products Intro: Product Name:4-(2-Methoxy-phenyl)-piperidine
CAS:58333-75-8
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Alchem Pharmtech,Inc.
Tel: 8485655694
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Products Intro: Product Name:4-(2-Methoxyphenyl)piperidine
CAS:58333-75-8
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-64427
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Products Intro: Product Name:4-(2-Methoxyphenyl)piperidine
CAS:58333-75-8
Purity:0.98 Package:1g;5g;25g;100;500g
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: CAS:58333-75-8
Purity:0.99 Package:1kg
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Products Intro: Product Name:4-(2-METHOXYPHENYL)PIPERIDINE
CAS:58333-75-8
Purity:98% Package:1KG;5USD

4-(2-METHOXYPHENYL)PIPERIDINE manufacturers

4-(2-METHOXYPHENYL)PIPERIDINE Basic information
Product Name:4-(2-METHOXYPHENYL)PIPERIDINE
Synonyms:4-(2-METHOXYPHENYL)PIPERIDINE;2-(Piperidin-4-yl)anisole;Piperidine,4-(2-methoxyphenyl)-;4-(2-Methoxyphenyl)
CAS:58333-75-8
MF:C12H17NO
MW:191.27
EINECS:
Product Categories:
Mol File:58333-75-8.mol
4-(2-METHOXYPHENYL)PIPERIDINE Structure
4-(2-METHOXYPHENYL)PIPERIDINE Chemical Properties
Melting point 54 °C
Boiling point 115-118 °C(Press: 1.1 Torr)
density 1.003±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka10.22±0.10(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-52/53
Safety Statements 26-36/37/39-61
Hazard Note Irritant
HS Code 2933399990
MSDS Information
4-(2-METHOXYPHENYL)PIPERIDINE Usage And Synthesis
Synthesis
1,1-Dimethylethyl 4-(2-methoxyphenyl)-1-piperidinecarboxylate

201609-29-2

4-(2-METHOXYPHENYL)PIPERIDINE

58333-75-8

General procedure for the synthesis of 4-(2-methoxyphenyl)piperidine-1-carboxylic acid tert-butyl ester from 4-(2-methoxyphenyl)piperidine-1-carboxylic acid: a solution of 4-(2-methoxyphenyl)piperidine-1-carboxylic acid tert-butyl ester (70 mg, 0.24 mmol) with 10% wet Pd/C (10 mg) in 10 mL of ethyl acetate was purged three times with N2 and then stirred in H2 atmosphere (50 psi) with stirring overnight. After completion of the reaction, the suspension was filtered and the filtrate was evaporated in vacuum to give 4-(2-methoxyphenyl)piperidine (70 mg, yield: 99%) as a colorless oil. 4-(2-methoxyphenyl)piperidine (70 mg, 0.24 mmol) was dissolved in 5 mL HCl/dioxane and stirred overnight at room temperature. After completion of the reaction, the solution was evaporated to dryness in vacuum. The solid was washed with ether to give 4-(2-methoxyphenyl)piperidine hydrochloride (35 mg, yield: 76%) as a white solid.

References[1] Patent: WO2014/100501, 2014, A1. Location in patent: Paragraph 00407
[2] Bioorganic and Medicinal Chemistry Letters, 1998, vol. 8, # 14, p. 1851 - 1856
[3] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8685 - 8699,15
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8685 - 8699
4-(2-METHOXYPHENYL)PIPERIDINE Preparation Products And Raw materials
Raw materials1,1-Dimethylethyl 4-(2-methoxyphenyl)-1-piperidinecarboxylate-->1,4-Dioxane-->Hydrochloric acid
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