HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842794Generated: November 1, 2026
Binap, (A+-)- → N-(2-(2,2,2-Trifluoroethoxy)phenyl)-4-piperidone propylene ketal
https://huagongshe.com/reaction/842794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 4-Piperidone propylene ketal | HCID 12954117 | — |
| Reactant | 1-Bromo-2-(2,2,2-trifluoroethoxy)benzene | HCID 22615479 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | N-(2-(2,2,2-Trifluoroethoxy)phenyl)-4-piperidone propylene ketal | HCID 57019377 | — |
Reaction Steps
A solution of 50 (1.786 g, 7.00 mmol) and 4-piperidone propylene ketal (2.645 g, 16.82 mmol) in toluene (30 mL) was treated with sodium tert-butoxide (1.88 g, 19.56 mmol), (S)-BINAP (44 mg, 0.07 mmol), and tris(dibenzylideneacetone)dipalladium(0) (32 mg, 0.035 mmol) at room temperature. The mixture was heated in an oil bath (80° C., 3 h). The mixture was diluted with ether and brine. The aqueous layer was extracted with two additional portions of ether and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. PCTLC (SiO2, 6 mm, 20% EtOAc-80% hexane) afforded the title compound (51).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376503B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-fb00847501dd46f78e336a2a664abbff |
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| Source note | uspto-grants-2002_04 |
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