HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042606Generated: October 26, 2026
Hydrochloric Acid → 4-(4,4,4-Trifluorobutoxy)benzoic acid
https://huagongshe.com/reaction/1042606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4,4,4-Trifluorobutan-1-ol | HCID 136307 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methylparaben | HCID 7456 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4,4,4-Trifluorobutoxy)benzoic acid | HCID 22361401 | 391.1% |
Reaction Steps
55.00 g (0.408 Mol) 4,4,4-trifluorobutan-1-ol are dissolved in 550 ml tetrahydrofurane, 142 ml (0.102 Mol) triethylamine are added at room temperature. 38 ml (0.490 Mol) methanesulfonyl chloride were added dropwise under nitrogen. The mixture is stirred for 1 h at 0-5° C. The beige suspension is Hyflo-filtrated and washed with tetrahydrofurane. The filtrate is concentrated. The residue is dissolved in 1.4 l 1-methyl-2-pyrrolidone 62.70 g (0.408 Mol) of methyl 4-hydroxybenzoate and 226.00 g (1.43 Mol) of potassium carbonate are added to the lightly brown solution. The reaction suspension is allowed to react at 80° C. for 14 h. 1 l (1.0 Mol) of a 1N NaOH solution is added to the above mixture. The suspension is heated at reflux temperature for 30 min until the reaction is completed. The reaction mixture is allowed to cool at room temperature and thrown in cold water. The solution is carefully acidified with a 25% HCl solution and is stirred for 15 min. The product is filtrated off, washed with water and dried overnight at room temperature under vacuum to give 99.00 g (98%) of 4-(4,4,4-trifluorobutoxy)benzoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557922B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-1aa37931c1574bb088fc082a6145921e |
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| Source note | uspto-grants-2013_10 |
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