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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511469Generated: November 4, 2026

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

https://huagongshe.com/reaction/1511469

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 tetrahydrofuran (17 mL) with n-BuLi (1.6 M in hexanes; 8.0 mmol) dropwise at −15° C. After 15 minutes at −15° C., a solution of N-(4-methoxy-2-methylbenzylidene)-cyclohexanamine (660 mg; 2.86 mmol) in tetrahydrofuran (3 mL) was added dropwise to give a purple solution. The reaction mixture was allowed to warm to 0° C. over a 20 minute period, then a solution of N-methyl-N-methoxycyclopropanecarboxamide (630 mg: 4.4 mmol) in tetrahydrofuran (2 mL) was added in one portion while at 0° C. The reaction mixture was kept at room temperature for 30 minutes and then added to saturated aqueous ammonium chloride. The solution was extracted with diethyl ether and the organic phase was washed with brine, dried and concentrated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211897B2
Source datasetuspto-grants-2012_07
ORD IDord-1a0edf2618a340c5b5b4573009b96e43
Source noteuspto-grants-2012_07