HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407479Generated: October 31, 2026
4-(Trifluoromethyl)benzoic acid → HCID 59509432, compound
https://huagongshe.com/reaction/2407479
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Trifluoromethyl)benzoic acid | HCID 9966 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 178513316 | HCID 178513316 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59509432 | HCID 59509432 | — |
Reaction Steps
A mixture of 4-trifluoromethylbenzoic acid (6 g, 0.032 mol), 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide (6.05 g, 0.0315 mol) and 1-hydroxy-benzotriazole hydrate (4.82 g, 0.032 mol) in N,N-dimethylformamide (30 mL) is stirred at room temperature for 30 minutes. N-Hydroxy-4-hydroxymethylbenzamidine (6.97 g, 90%, 0.038 mol) is added and the reaction mixture is heated at reflux for 3 hrs, then allowed to come to room temperature and solvent is removed under reduced pressure. An aqueous solution (100 mL) of sodium bicarbonate is added to the residue and the aqueous layer is extracted with ethyl acetate (2×100 mL). Combined organic layers are dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue is purified by column chromatography (silica gel 230-400 mesh, n-hexane:ethyl acetate, 65:35) to give 4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]phenylmethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809539B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-95a3d25684ad4fe6a9af7db3b48b0426 |
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| Source note | uspto-grants-2014_08 |
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