HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473360Generated: October 30, 2026
1-Chloro-1-(4-methoxyphenyl)-1-trifluoromethylethane → 1-Methoxy-4-(1,1,1-trifluoro-2-methylpropan-2-yl)benzene
https://huagongshe.com/reaction/473360
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-1-(4-methoxyphenyl)-1-trifluoromethylethane | HCID 13885600 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-Methoxy-4-(1,1,1-trifluoro-2-methylpropan-2-yl)benzene | HCID 18333624 | — |
Reaction Steps
A solution of 1-(2-chloro-1,1,1-trifluoropropan-2-yl)-4-methoxybenzene (18.0 g, 75 mmol) in 400 ml of hexanes was treated with trimethylaluminum (151 ml, 302 mmol) (2.0 M in heptane) at rt and the resulting mixture was heated at 95° C. overnight. The reaction mixture was cooled in an ice-water bath, conc. HCl was added to the reaction mixture dropwise. Fumes were generated. After about 10 ml of conc. HCl was added, more rapid addition of acid was possible due to the near complete quenching of the unreacted AlMe3. After addition of 100 ml of conc. HCl, 250 ml of H2O was added and the mixture was stirred vigorously for 1 h. The layers were separated. The org layer was dried (Na2SO4) and concentrated to give the title compound as an oil, which solidified upon drying on the vac line.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633315B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-b3bf30cb2a3a4f228191372036b0d875 |
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| Source note | uspto-grants-2014_01 |
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