HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504059Generated: October 26, 2026
Acetyl chloride → 1-[2-Methoxy-5-(pentafluoroethyl)phenyl]ethanone
https://huagongshe.com/reaction/504059
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1-Methoxy-4-(pentafluoroethyl)benzene | HCID 12871966 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-[2-Methoxy-5-(pentafluoroethyl)phenyl]ethanone | HCID 86088705 | — |
Reaction Steps
7.4 ml of BuLi at 2.5M in hexane are added, at −70° C., to a solution of 3.5 g of 1-methoxy-4-pentafluoroethylbenzene in 50 ml of anhydrous THF. The medium is stirred for 30 minutes at −70° C. and then for 45 minutes at 0° C. 15.5 ml of a 1M solution of zinc chloride in ether are then added. After stirring for 10 minutes at 0° C., 1.33 ml of acetyl chloride are added. The medium is then deoxygenated with nitrogen and 332 mg of benzyl(chloro)bis(triphenylphosphine)palladium in 5 ml of anhydrous THF are introduced. The medium is stirred for 2 hours 30 minutes at 0° C. and then for 72 hours at RT. The medium is poured onto 2.5M HCl solution and then extracted with ether. The organic phase is washed with 5% NaHCO3 in water, with water and then with saturated NaCl solution. After drying over MgSO4 and evaporation, the crude product is purifed by flash chromatography on silica to give 2.25 g of a white solid. m.p.=47° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777041B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-3470a3f5deaf4aaaa4a0844b60602a50 |
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| Source note | uspto-grants-2010_08 |
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