Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | alpha,alpha,alpha,3-Tetrafluorotoluene | HCID 67867 | — |
| Reactant | HCID 11715514 | HCID 11715514 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14649985 | HCID 14649985 | 20.9% |
Reaction Steps
A stirred suspension of sodium hydride (60% in oil, 1.8 g) in 35 ml of dimethylformamide was treated with a solution of 9.00 g of 1-acetyl-4-hydroxy-4-phenylpiperidine in 100 ml of dimethylformamide and heated at 70° C. until evolution of gas had ceased. A solution of 7.38 g of 3-fluorobenzotrifluoride in 20 ml of dimethylformamide was added, dropwise, and the reaction allowed to proceed at 70° C. for 20 hours. The reaction mixture was then poured into an ice/water mixture and the aqueous suspension extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered and concentrated to an oil. High pressure liquid chromatography of the oil (silica gel; elution with 50% ethyl acetate/dichloromethane) afforded 3.11 g (20.90%) of 1-acetyl-4-phenyl-4-(3-trifluoromethylphenoxy)piperidine, m.p. 100°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853384 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-146d875aa3d048ac942755af437b8b16 |
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| Source note | uspto-grants-1989_08 |
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