HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089916Generated: October 31, 2026
2,2,6,6-Tetramethylpiperidine → HCID 178418821, compound
https://huagongshe.com/reaction/1089916
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | 1-(Phenylsulfonyl)-1H-pyrrolo[3,2-c]pyridine | HCID 11010657 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506647 | HCID 178506647 | — |
| Catalyst | HCID 178526220 | HCID 178526220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178418821 | HCID 178418821 | 100% |
Reaction Steps
A solution of 0.15 mole of lithium 2,2,6,6-tetramethylpiperidide is prepared by the addition of 0.15 mole of n-butyllithium to 0.15 mole of 2,2,6,6-tetramethylpiperidine in 120 ml of tetrahydrofuran at a temperature lower than -20° C. This solution is then added over a period of a few minutes to 0.1 mole of 1-benzenesulfonyl 5-aza indole cooled to -70° C. while maintaining this temperature throughout the addition. 0.15 mole of anhydrous manganous chloride is then added to the solution of 1-benzenesulfonyl 2-lithio 5-aza indole. The temperature of the medium is then brought from -65° C. to -25° C. in order to bring the exchange reaction to completion and obtain a solution of the desired manganous derivative which is used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05079363 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-7c20623e91274cff997eeb6cac14a0f0 |
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| Source note | uspto-grants-1992_01 |
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