HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558481Generated: October 28, 2026
Hydrochloric Acid → 1-[3-Ethoxy-4-(trifluoromethyl)phenyl]ethanone
https://huagongshe.com/reaction/558481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86607991 | HCID 86607991 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-[3-Ethoxy-4-(trifluoromethyl)phenyl]ethanone | HCID 66650336 | — |
Reaction Steps
To a solution of 3-ethoxy-N-methoxy-N-methyl-4-trifluoromethyl-benzamide from step 7 (15.96 g, 58 mmol) in THF (182 mL) at −5° C. was added methylmagnesium bromide (3 M in Et2O, 38.37 mL, 115 mmol). The mixture was stirred at 0° C. for 15 min, then warmed up to 23° C., stirring was continued for further 3 h at 23° C. Cooled to 0° C., 1 N HCl (274 mL) was added dropwise, stirring was continued at 23° C. for 15 min, the mixture was diluted with TBME, the phases were separated, the organic layer was washed with water and brine, dried over MgSO4. Removal of the solvent in vacuum left a yellow solid (13.10 g, 98%), which was used without further purification. MS (EI) 232.2 [M].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063048B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-1a1dffd480794afb8305d67bb82f4eff |
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| Source note | uspto-grants-2011_11 |
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