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3-(1-Piperidinylmethyl)phenol

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3-(1-Piperidinylmethyl)phenol Basic information
Product Name:3-(1-Piperidinylmethyl)phenol
Synonyms:(4-FLUORO-PHENYL)-PIPERIDIN-4-YL-METHANONE HYDROCHLORIDE;Roxatidine Impurity 4;1-(3-HYDROXYPHENYLMETHYL)PIPERIDINE;3-(1-PIPERIDINOMETHYL)PHENOL;3-(1-PIPERIDINYLMETHYL)PHENOL;BUTTPARK 99\50-17;Piperidinol;4-(4-FLUOROBENZOYL)PIPERIDINE HCL
CAS:73279-04-6
MF:C12H17NO
MW:191.27
EINECS:
Product Categories:(intermediate of roxatidine)
Mol File:73279-04-6.mol
3-(1-Piperidinylmethyl)phenol Structure
3-(1-Piperidinylmethyl)phenol Chemical Properties
Melting point 137-138°C
Boiling point 308.1±17.0 °C(Predicted)
density 1.097±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka9.97±0.10(Predicted)
color White to Almost white
InChIInChI=1S/C12H17NO/c14-12-6-4-5-11(9-12)10-13-7-2-1-3-8-13/h4-6,9,14H,1-3,7-8,10H2
InChIKeyORGBERFQYFWYGX-UHFFFAOYSA-N
SMILESC1(O)=CC=CC(CN2CCCCC2)=C1
CAS DataBase Reference73279-04-6(CAS DataBase Reference)
Safety Information
HS Code 2933399990
MSDS Information
ProviderLanguage
ALFA English
3-(1-Piperidinylmethyl)phenol Usage And Synthesis
Synthesis
Piperidine

110-89-4

3-Hydroxybenzaldehyde

100-83-4

3-(1-Piperidinylmethyl)phenol

73279-04-6

In a three-necked flask equipped with a stirrer, condenser tube and thermometer, add 2.4 g of m-hydroxybenzaldehyde dissolved in 40 mL of formic acid with stirring. The temperature was controlled to be below 60 °C and 4.2 g of hexahydropyridine was slowly added dropwise. After the dropwise addition was completed, the temperature was raised to 110 °C and the reaction was refluxed for 2 h (the progress of the reaction was monitored by thin layer chromatography). Upon completion of the reaction, the reaction solution was diluted with 150 mL of water and cooled to 15 °C. Decolorization was carried out by adding 0.1 g of activated carbon and filtered. The pH of the filtrate was adjusted with 12% ammonia to 8.5. allowed to stand and crystallized at 10 °C. The crystals were collected by filtration, washed with cold water and dried to give Intermediate III-1 (3-(1-piperidinylmethyl)phenol) 3.0 g as yellow crystals in 78% yield.

References[1] Arzneimittel-Forschung/Drug Research, 1985, vol. 35, # 7, p. 1025 - 1029
[2] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 4, p. 989 - 994
[3] ChemMedChem, 2015, vol. 10, # 1, p. 83 - 93
[4] Patent: CN103626722, 2016, B. Location in patent: Paragraph 0049-0052
[5] Synthetic Communications, 1999, vol. 29, # 1, p. 15 - 20
3-(1-Piperidinylmethyl)phenol Preparation Products And Raw materials
Raw materials3-(Piperidin-1-ylmethyl)aniline-->Piperidine, 1-[(3-methoxyphenyl)methyl]--->Piperidine-->3-Hydroxybenzaldehyde
Preparation ProductsRoxatidine
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