HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184069Generated: October 30, 2026
Aniline → 2-(4-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol
https://huagongshe.com/reaction/2184069
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | Hexafluoroacetone trihydrate | HCID 36719 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol | HCID 577801 | 45.2% |
Reaction Steps
A neat solution of aniline (4.3 mL, 47 mmol) and p-toluenesulfonic acid monohydrate (85 mg, 0.45 mmol) in a round bottom flask equipped with a reflux condenser was heated to 90° C. and hexafluoroacetone trihydrate (7 mL, 50 mmol) added over 15 minutes via syringe. Following addition, the temperature was increased to 130° C. and the resulting solution stirred over 18 h. The reaction mixture was cooled to room temperature and diluted with ethyl acetate. The organics were washed with saturated NaHCO3 solution then brine. The solution was dried over MgSO4 and the solvent removed in vacuo. The residue was purified by flash chromatography (4:1 hexanes/EtOAc) to give the title product as a white crystalline solid (5.5 g, 45%). MS (ES+) m/z 260 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900244B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-6741d6f1d4f04ec2b64becda6c92adf4 |
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| Source note | uspto-grants-2005_05 |
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