HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397255Generated: October 30, 2026
Allyl bromide → 4-Allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide
https://huagongshe.com/reaction/2397255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Piperidine, 2,2,6,6-tetramethyl-4-(2-propen-1-yloxy)- | HCID 11117001 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide | HCID 19736221 | — |
Reaction Steps
A mixture of 9.87 parts of 4-allyloxy-2,2,6,6-tetramethylpiperidine and 3.03 parts of allyl bromide was heated at 90° C. for 96 hours. Ether was added to the cooled reaction mixture and the 4-allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide formed during the reaction was filtered off. The ether solvent was removed by distillation under reduced pressure and the residue purified by chromatography to give 4-allyloxy-1-allyl-2,2,6,6-tetramethylpiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04021432 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-49a296defce54e08961e331476fba744 |
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| Source note | uspto-grants-1977_05 |
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