Benzoic acid, 4-(5-heptyl-2-pyrimidinyl)-, 4-[3-(trifluoromethyl)heptyl]phenyl ester

Base Information

Chemical Name:Benzoic acid, 4-(5-heptyl-2-pyrimidinyl)-, 4-[3-(trifluoromethyl)heptyl]phenyl ester
CAS No.:138824-31-4
Molecular Formula:C₃₂H₃₉F₃N₂O₂
Molecular Weight:540.669
Hs Code.:

Synonyms:

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Chemical Property of Benzoic acid, 4-(5-heptyl-2-pyrimidinyl)-, 4-[3-(trifluoromethyl)heptyl]phenyl ester

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Technology Process of Benzoic acid, 4-(5-heptyl-2-pyrimidinyl)-, 4-[3-(trifluoromethyl)heptyl]phenyl ester

There total 7 articles about Benzoic acid, 4-(5-heptyl-2-pyrimidinyl)-, 4-[3-(trifluoromethyl)heptyl]phenyl ester 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:

: 360-34-9
1,1,1-trifluoro-2-hexanone

: 138824-31-4
4-(5-Heptyl-pyrimidin-2-yl)-benzoic acid 4-(3-trifluoromethyl-heptyl)-phenyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1) NaOEt / 1) CH₂Cl₂, room temp., 2) room temp.

2: H₂ / 5percent Pd/C / methanol

3: NaOH / methanol; H₂O / Heating

4: thionyl chloride / 80 °C

5: CS₂, AlCl₃ / Heating

6: LiAlH₄, AlCl₃ / diethyl ether / Heating

7: 1) 1,4-diazabicyclo<2.2.2>octane, 2) NaH / 1) benzene, 50 deg C, 2) a) room temp., b) reflux

With 1,4-diaza-bicyclo[2.2.2]octane; carbon disulfide; sodium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; thionyl chloride; hydrogen; sodium ethanolate; sodium hydride; palladium on activated charcoal; In methanol; diethyl ether; water;

Reference yield:

: 121215-01-8
(Z)-3-Trifluoromethyl-hept-2-enoic acid ethyl ester

: 138824-31-4
4-(5-Heptyl-pyrimidin-2-yl)-benzoic acid 4-(3-trifluoromethyl-heptyl)-phenyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: H₂ / 5percent Pd/C / methanol

2: NaOH / methanol; H₂O / Heating

3: thionyl chloride / 80 °C

4: CS₂, AlCl₃ / Heating

5: LiAlH₄, AlCl₃ / diethyl ether / Heating

6: 1) 1,4-diazabicyclo<2.2.2>octane, 2) NaH / 1) benzene, 50 deg C, 2) a) room temp., b) reflux

With 1,4-diaza-bicyclo[2.2.2]octane; carbon disulfide; sodium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; thionyl chloride; hydrogen; sodium hydride; palladium on activated charcoal; In methanol; diethyl ether; water;

Reference yield:

: 115619-31-3,121214-69-5,138863-70-4
3-Trifluoromethyl-heptanoic acid

: 138824-31-4
4-(5-Heptyl-pyrimidin-2-yl)-benzoic acid 4-(3-trifluoromethyl-heptyl)-phenyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 80 °C

2: CS₂, AlCl₃ / Heating

3: LiAlH₄, AlCl₃ / diethyl ether / Heating

4: 1) 1,4-diazabicyclo<2.2.2>octane, 2) NaH / 1) benzene, 50 deg C, 2) a) room temp., b) reflux

With 1,4-diaza-bicyclo[2.2.2]octane; carbon disulfide; lithium aluminium tetrahydride; aluminium trichloride; thionyl chloride; sodium hydride; In diethyl ether;