HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597547Generated: October 30, 2026
1-Bromododecane → HCID 21532980, compound
https://huagongshe.com/reaction/597547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21532980 | HCID 21532980 | — |
Reaction Steps
A mixture of 15.7 parts of 2,2,6,6-tetramethylpiperidin-4-ol and 12.5 parts of n-dodecyl bromide in 50 parts of ethyl alcohol was heated under reflux conditions for 72 hours. The cooled reaction mixture was filtered to remove 2,2,6,6-tetramethylpiperidin-4-ol hydrobromide formed during the reaction and the ethyl alcohol solvent was removed by distillation under reduced pressure. The residue was treated with petroleum under (b.p. 40°-60°C) and filtered to remove the unreacted 2,2,6,6-tetramethylpiperidin-4-ol and the petroleum ether solvent was removed by distillation under reduced pressure. Fractional distillation of the residue gave 1-n-dodecyl-2,2,6,6-tetramethylpiperidin-4-ol having a melting point of 41°-2°C and the following elemental analysis by weight:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04014887 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-114a87da323340c78ecb48e6ebd53b91 |
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| Source note | uspto-grants-1977_03 |
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