Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate

Base Information

Chemical Name:Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate
CAS No.:107971-44-8
Molecular Formula:C₁₇H₂₁NO₄
Molecular Weight:303.358
Hs Code.:
DSSTox Substance ID:DTXSID401143887

Synonyms:DTXSID401143887;Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate;107971-44-8

Suppliers and Price of Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate

Supply Marketing:

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

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Chemical Property of Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:303.14705815
Heavy Atom Count:22
Complexity:402

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(N(C=CC1=O)C(=O)OCC2=CC=CC=C2)CCCCO

Technology Process of Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate

There total 3 articles about Phenylmethyl 3,4-dihydro-2-(4-hydroxybutyl)-4-oxo-1(2H)-pyridinecarboxylate 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:

: 1122-96-9
4-methoxypyridine N-oxide

: 107971-44-8
N-<(benzyloxy)carbonyl>-2-(4-hydroxybutyl)-2,3-dihydro-4-pyridone

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 5percent Pd/C / ethanol

2: 1.) THF, -23 deg C 2.) acidic workup

With hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1016/S0040-4039(00)85000-5