4-(Piperidin-1-ylmethyl)phenol

Base Information

• Chemical Name: 4-(Piperidin-1-ylmethyl)phenol
• CAS No.: 73152-41-7
• Molecular Formula: C12H17NO
• Molecular Weight: 191.273
• Hs Code.: 2933399990
• DSSTox Substance ID: DTXSID50469800
• Nikkaji Number: J1.746.325J
• Wikidata: Q82297668
• Mol file: 73152-41-7.mol

Synonyms:4-(Piperidin-1-ylmethyl)phenol;73152-41-7;4-(1-Piperidinylmethyl)-phenol;4-Piperidin-1-ylmethyl-phenol;Phenol, 4-(1-piperidinylmethyl)-;p-(piperidinomethyl)phenol;SCHEMBL1888525;DTXSID50469800;BPCKWVMOXOYTQI-UHFFFAOYSA-N;4-((piperidin-1-yl)methyl)phenol;MFCD18453499;AKOS006280709;SB42647;BS-18017;CS-0163021;D83484;A1-06228

Chemical Property of 4-(Piperidin-1-ylmethyl)phenol

Chemical Property:

• PSA: 23.47000
• LogP: 2.31600
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 191.131014166
• Heavy Atom Count: 14
• Complexity: 158

Purity/Quality:

99% ^*data from raw suppliers

4-(Piperidin-1-ylmethyl)phenol 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(CC1)CC2=CC=C(C=C2)O

Technology Process of 4-(Piperidin-1-ylmethyl)phenol

There total 7 articles about 4-(Piperidin-1-ylmethyl)phenol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

piperidine (110-89-4) + 4-hydroxy-benzaldehyde (123-08-0,65581-83-1) → 4-(piperidin-1-ylmethyl)phenol (73152-41-7)

Guidance literature:

With sodium tris(acetoxy)borohydride; In dichloromethane;

DOI:10.1016/j.bmcl.2005.10.087

Reference yield: 83.0%

4-(1-piperidinylmethyl)phenylmagnesium bromide → 4-(piperidin-1-ylmethyl)phenol (73152-41-7)

Guidance literature:

With air; In tetrahydrofuran; at -25 ℃; for 0.0566667h; under 12929 Torr; Green chemistry;

DOI:10.1002/anie.201310572

Reference yield: 74.0%

(4-hydroxyphenyl)(piperidin-1-yl)methanone (58547-68-5) → 4-(piperidin-1-ylmethyl)phenol (73152-41-7)

Guidance literature:

With titanium tetrachloride; magnesium; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1002/adsc.201300355

upstream raw materials:

piperidine

4-hydroxy-benzaldehyde

4-methoxy-benzaldehyde

(4-hydroxyphenyl)(piperidin-1-yl)methanone

Downstream raw materials:

2-[3-(4-Piperidin-1-ylmethyl-phenoxy)-propyl]-isoindole-1,3-dione

1-[2-(4-Piperidin-1-ylmethyl-phenoxy)-ethyl]-4-(1-trityl-1H-imidazol-4-ylmethyl)-piperidine

1-[3-(4-Piperidin-1-ylmethyl-phenoxy)-propyl]-4-(1-trityl-1H-imidazol-4-ylmethyl)-piperidine

4-(4-piperidin-1-ylmethyl-phenoxy)-butyric acid ethyl ester