Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 86734708 | HCID 86734708 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 70529415 | HCID 70529415 | — |
Reaction Steps
A mixture of 28.3 parts of 2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate and 8.55 parts of benzyl bromide was stirred and heated at 105° C. for 72 hours. Ether was added to the cooled reaction mixture and the 2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate hydrobromide formed during the reaction was filtered off. The ether solvent was removed by distillation under reduced pressure and the residue distilled under reduced pressure to give 16.40 parts of 1-benzyl-2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate having a boiling point of 180° C. at 0.1 mm of Hg and the following elemental analysis by weight:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE031342 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-bda559ca454f412784e939ee280dd1ba |
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| Source note | uspto-grants-1983_08 |
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