5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

Base Information

Chemical Name:5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione
CAS No.:1281859-94-6
Molecular Formula:C₂₁H₂₁FN₂O₃
Molecular Weight:368.408
Hs Code.:

Synonyms:5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

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Chemical Property of 5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

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Technology Process of 5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

There total 4 articles about 5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione 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:

: 1313716-68-5
5-benzyl-6-ethylpyrimidine-2,4(1H,3H)-dione

: 104620-66-8
1-(chloromethoxymethyl)-4-fluorobenzene

: 1281859-94-6
5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

Guidance literature:: With N,O-bis-(trimethylsilyl)-acetamide; tetra-(n-butyl)ammonium iodide; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1021/jm1014378

Reference yield:

: 459-56-3
4-fluorobenzylic alcohol

: 1281859-94-6
5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

Guidance literature:: Multi-step reaction with 2 steps

1: chloro-trimethyl-silane / 20 °C / Inert atmosphere

2: N,O-bis-(trimethylsilyl)-acetamide; tetra-(n-butyl)ammonium iodide / dichloromethane / 20 °C / Inert atmosphere

With chloro-trimethyl-silane; N,O-bis-(trimethylsilyl)-acetamide; tetra-(n-butyl)ammonium iodide; In dichloromethane;
DOI:10.1021/jm1014378

Reference yield:

: C₁₃H₁₄N₂OS

: 1281859-94-6
5-benzyl-6-ethyl-1-(((4-fluorobenzyl)oxy)methyl)pyrimidine-2,4(1H,3H)- dione

Guidance literature:: Multi-step reaction with 2 steps

1.1: chloroacetic acid; acetic acid / water / Reflux

2.1: N,O-bis-(trimethylsilyl)-acetamide / dichloromethane / 0.5 h / 20 °C / Inert atmosphere

2.2: Inert atmosphere

With N,O-bis-(trimethylsilyl)-acetamide; acetic acid; chloroacetic acid; In dichloromethane; water;
DOI:10.1016/j.ejmech.2018.07.035