2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

Base Information

Chemical Name:2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone
CAS No.:1380429-73-1
Molecular Formula:C₁₉H₁₄ClF₃N₂O₃S
Molecular Weight:442.846
Hs Code.:

Synonyms:2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

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Chemical Property of 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

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Technology Process of 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

There total 4 articles about 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone 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: 42.7%

: 1380429-72-0
ethyl 2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-4-oxo-1,4-dihydro-5-pyrimidinecarboxylate

: 1380429-73-1
2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

Guidance literature:: With dimethylsulfide borane complex; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 1.5h; Inert atmosphere;

Reference yield:

: 6294-93-5
4-chloro-3-trifluoromethylphenol

: 1380429-73-1
2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 0.33 h / 120 °C / Microwave irradiation

2: methanol; sodium tetrahydroborate / 20 °C

3: thionyl chloride / dichloromethane / 1.5 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C / Microwave irradiation

5: dimethylsulfide borane complex / tetrahydrofuran; toluene / 1.5 h / 0 - 20 °C / Inert atmosphere

With methanol; sodium tetrahydroborate; thionyl chloride; dimethylsulfide borane complex; potassium carbonate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1369255-78-6
1-chloro-4-(4-(chloromethyl)phenoxy)-2-(trifluoromethyl)benzene

: 1380429-73-1
2-{[(4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}phenyl)methyl]thio}-5-(hydroxymethyl)-4(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C / Microwave irradiation

2: dimethylsulfide borane complex / tetrahydrofuran; toluene / 1.5 h / 0 - 20 °C / Inert atmosphere

With dimethylsulfide borane complex; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; toluene;