Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591869Generated: October 31, 2026

2,2,6,6-Tetramethylpiperidine → HCID 66938504, compound

https://huagongshe.com/reaction/1591869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
ReactantN-[(2-fluorophenyl)methyl]-1-methylpiperidin-4-amineHCID 781972—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66938504HCID 6693850435.5%

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) portionwise 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291632B2
Source datasetuspto-grants-2007_11
ORD IDord-5c6f2d107310466197a3b690cdc5651f
Source noteuspto-grants-2007_11