HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520264Generated: November 3, 2026
Hydrochloric Acid → 4-((4,4,4-Trifluoro-1-(2-methyl-4-(5-(trifluoromethyl)pyridin-2-yl)phenyl)butyl)amino)benzoic acid
https://huagongshe.com/reaction/1520264
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-(5,5,5-trifluoro-2-(2-methyl-4-(5-(trifluoromethyl)pyridin-2-yl)phenyl)pentyl)benzoate | HCID 117839891 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-((4,4,4-Trifluoro-1-(2-methyl-4-(5-(trifluoromethyl)pyridin-2-yl)phenyl)butyl)amino)benzoic acid | HCID 117839916 | — |
Reaction Steps
A reaction mixture of methyl 4-(5,5,5-trifluoro-2-(2-methyl-4-(5-(trifluoromethyl)pyridin-2-yl)phenyl)pentyl)benzoate (0.520 g), 1M aqueous sodium hydroxide solution (4.2 mL), THF (4 mL) and methanol (4 mL) was stirred at 70° C. overnight. The reaction mixture was neutralized with 1M hydrochloric acid at 0° C., and extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (0.504 g). This compound was used in step D without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073864B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-882c01ebabd54c29aa9e55a6e169425f |
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| Source note | uspto-grants-2015_07 |
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