HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,6,6-Tetramethylpiperidine → HCID 66938504, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | 1,2-Dibromo-1,1,2,2-tetrachloroethane | HCID 69426 | — |
| Reactant | N-[(2-fluorophenyl)methyl]-1-methylpiperidin-4-amine | HCID 781972 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66938504 | HCID 66938504 | 35.5% |
Reaction Steps
Add n-butyl lithium (1.6 M in hexanes, 4.3 mL) into a solution of 2,2,6,6-tetramethyl-piperidine (0.97 g) in THF (10 mL) at −78° C. and stir for 30 minutes. Add a solution of 1-methyl-4-(N-(2-fluorophenyl)methylamino)piperidine (Preparation 23, 1.02 g) in THF (10 mL) portion wise and stir for 10 minutes. Add 1,2-dibromo-1,1,2,2-tetrachloroethane (1.50 g) in THF (10 mL) dropwise and stir for 1 hr. Remove the cooling bath and stir for 30 minutes. Partition between ethyl acetate and saturated aqueous NaCl, dry over anhydrous sodium sulfate, evaporate and purify on a silica gel column (110 g), using a gradient of dichloromethane-2M NH3 in methanol to give 0.49 g of the title intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803813B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-b94a9e40c0d7401b936318919a0eb044 |
| Source note | uspto-grants-2010_09 |