5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

Base Information

Chemical Name:5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one
CAS No.:374627-58-4
Molecular Formula:C₁₂H₉F₃N₂O₃
Molecular Weight:286.21
Hs Code.:

Synonyms:5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

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

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Chemical Property of 5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

Chemical Property:

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Technology Process of 5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

There total 3 articles about 5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one 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: 76.0%

: 251984-01-7
5-benzoyl-4-trifluoromethyl-2-methoxypyrimidine

: 374627-58-4
5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

Guidance literature:: With hydrogen bromide; In acetic acid; at 25 ℃; for 24h;
DOI:10.3987/com-99-8635

Reference yield:

: 1131-80-2,1201-93-0,31919-75-2
(E)-3-(N,N-dimethylamino)-1-phenyl-2-propen-1-one

: 374627-58-4
5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / CH₂Cl₂ / 72 h / 25 °C

2: 63 percent / K₂CO₃ / acetonitrile / 20 h / 25 °C

3: 76 percent / 33 percent HBr / acetic acid / 24 h / 25 °C

With hydrogen bromide; potassium carbonate; In dichloromethane; acetic acid; acetonitrile; 1: Acylation / 2: Cyclization / 3: Hydrolysis;
DOI:10.3987/com-99-8635

Reference yield:

: 3-benzoyl-1,1,1-trifluoro-4-N,N-dimethylaminobut-3-en-2-one

: 374627-58-4
5-benzoyl-4-trifluoromethyl-4-hydroxy-1,2,3,4-tetrahydropyrimidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / K₂CO₃ / acetonitrile / 20 h / 25 °C

2: 76 percent / 33 percent HBr / acetic acid / 24 h / 25 °C

With hydrogen bromide; potassium carbonate; In acetic acid; acetonitrile; 1: Cyclization / 2: Hydrolysis;
DOI:10.3987/com-99-8635