Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | 4-Piperidinol, 1,2,2,6,6-pentamethyl- | HCID 75472 | — |
| Reactant | HCID 20449612 | HCID 20449612 | — |
| Solvent | Mesitylene | HCID 7947 | — |
| Product | HCID 20449618 | HCID 20449618 | — |
Reaction Steps
42.7 g of ethyl 4,4-di-(4-hydroxy-3-t-butyl-phenyl)-valerate and 17.1 g of 1,2,2,6,6-pentamethyl-4-hydroxy-piperidine in 120 ml of mesitylene, with the addition of 100 mg of lithium amide as the catalyst, are heated to 160° C. in a nitrogen atmosphere for 5 hours, whilst stirring. During this time, the ethanol formed distils off in the stream of nitrogen and can be measured in a cold trap. After cooling, 100 ml of toluene are added to the batch and the solution is washed with water, dried with calcium chloride and evaporated in vacuo. The crystalline residue is recrystallised from acetonitrile or chlorobenzene. In this way 1,2,2,6,6-pentamethyl-piperidin-4-yl 4,4-di-(4-hydroxy-3-t-butyl-phenyl)-valerate (stabiliser no. 2) is obtained as a white crystalline powder with a melting point of 203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04197236 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-46843a188d0845a9b348e7c2e0fd695d |
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| Source note | uspto-grants-1980_04 |
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