Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895867Generated: November 1, 2026

2,2,6,6-Tetramethylpiperidine → HCID 178418821, compound

https://huagongshe.com/reaction/1895867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-Methoxy-N-methylcyclopropanecarboxamideHCID 15643267—
Reactant(E)-N-Cyclohexyl-1-(4-methoxy-2-methylphenyl)methanimineHCID 57893115—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178418821HCID 178418821—

Reaction Conditions

Temperature0 °C

Reaction Steps

Lithium tetramethylpiperidide was prepared by the treatment of 2,2,6,6-tetramethylpiperidine (1.0 g; 7.0 mmol) in THF (17 mL) with n-BuLi (1.6 M in hexanes; 8.0 mmol) dropwise at −15° C. After 15 min at −15° C., a solution of cyclohexyl(4-methoxy-2-methylbenzylidene)amine (660 mg; 2.86 mmol) in THF (3 mL) was added dropwise to give a purple solution. The reaction mixture was allowed to warm to 0° C. over a 20-min period then a solution of N-methyl-N-methoxycyclopropanecarboxamide (630 mg: 4.4 mmol) in THF (2 mL) was added in one portion while at 0° C. The reaction mixture was kept at room temperature for 30 min and then added to saturated aq. NH4Cl. The solution was extracted with diethyl ether and the organic phase was washed with saturated aq. NaCl, dried and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518874B2
Source datasetuspto-grants-2013_08
ORD IDord-98d2ddfd175f4c13a424e93d674b30ab
Source noteuspto-grants-2013_08