HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675646Generated: October 31, 2026
P-Xylene → 2-(2,5-Dimethylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol
https://huagongshe.com/reaction/1675646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Catalyst | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2-(2,5-Dimethylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol | HCID 2775085 | 88.2% |
Reaction Steps
A 1 L reactor was charged under nitrogen with 200.0 g (1.88 mol) of p-xylene and 12.5 g (0.094 mol/0.06 eq) of aluminum chloride, followed by adjusting the inside temperature to 18° C. Then, 327.7 g (1.97 mol/1.06 eq) of hexafluoroacetone was introduced in a temperature range of 18-25° C. After the introduction, stirring was conducted at room temperature for 3 hr. Then, 200 mL of 10% hydrochloric acid was added. The resulting aqueous layer was extracted two times with 50 mL of chloroform. The resulting organic layers were combined together, followed by removing water with anhydrous magnesium sulfate, filtration, concentration, and vacuum distillation, thereby obtaining 451.3 g of 2-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]-1,4-dimethylbenzene represented by the following formula. Upon this, purity was 92%, and yield was 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003749B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-e5287b55771349f9ae31046cec9ec7a3 |
|---|
| Source note | uspto-grants-2011_08 |
|---|