HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821602Generated: October 30, 2026
2,2,6,6-Tetramethylpiperidine → HCID 178418821, compound
https://huagongshe.com/reaction/1821602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-Methoxy-N-methylcyclopropanecarboxamide | HCID 15643267 | — |
| Reactant | (E)-N-Cyclohexyl-1-(4-methoxy-2-methylphenyl)methanimine | HCID 57893115 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178418821 | HCID 178418821 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608592B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-2ab7dbd4e7c34e89a6639c144c9f2b8b |
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| Source note | uspto-grants-2009_10 |
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