1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Base Information

Chemical Name:1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate
CAS No.:117023-31-1
Molecular Formula:C₂H₂O₄*C₃₂H₃₉NO₆
Molecular Weight:623.7
Hs Code.:

Synonyms:1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Suppliers and Price of 1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

There total 5 articles about 1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate 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:

: 104-92-7
1-bromo-4-methoxy-benzene

: 117023-31-1
1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Guidance literature:: Multi-step reaction with 3 steps

1: 1) Mg / 1) THF, reflux; 2) THF, room temperature, overnight

2: 30 percent / H₂ / 5percent Pd/C / ethanol / 70 °C / 2585.7 Torr

3: 53 percent / 1) Na₂CO₃, KI / 1) n-butanol, reflux

With hydrogen; sodium carbonate; magnesium; potassium iodide; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00121a022

Reference yield:

: 24228-40-8
N-benzyl isonipecotic acid ethyl ester

: 117023-31-1
1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Guidance literature:: Multi-step reaction with 3 steps

1: 1) Mg / 1) THF, reflux; 2) THF, room temperature, overnight

2: 30 percent / H₂ / 5percent Pd/C / ethanol / 70 °C / 2585.7 Torr

3: 53 percent / 1) Na₂CO₃, KI / 1) n-butanol, reflux

With hydrogen; sodium carbonate; magnesium; potassium iodide; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00121a022

Reference yield:

: 117022-62-5
α,α-bis(4-methoxyphenyl)-1-(phenylmethyl)-4-piperidinemethanol

: 117023-31-1
1-[4-[3-[4-[Bis(4-methoxyphenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone oxalate

Guidance literature:: Multi-step reaction with 2 steps

1: 30 percent / H₂ / 5percent Pd/C / ethanol / 70 °C / 2585.7 Torr

2: 53 percent / 1) Na₂CO₃, KI / 1) n-butanol, reflux

With hydrogen; sodium carbonate; potassium iodide; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00121a022