Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Oxo-2-phenylacetyl chloride | HCID 11084294 | — |
| Reactant | HCID 19991754 | HCID 19991754 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22153826 | HCID 22153826 | 76% |
Reaction Steps
24.1 g (0.1 mole) of 4-hexyloxy-2,2,6,6-tetramethylpiperidine are dissolved in 100 ml of absolute methylene chloride. To this solution are added 15.2 g (0.15 mole) of absolute triethylamine and the whole solution is cooled to -10° C. At this temperature a solution of 16.8 g (0.1 mole) of phenylglyoxylyl chloride in 100 ml of methylene chloride is slowly added dropwise. When this addition is complete, the reaction mixture is allowed to warm to room temperature and stirred for about 4 hours. Precipitated hydrochloride is removed by filtration and the solution is clarified by filtration over a small amount of silica gel and concentrated by evaporation, affording 28.4 g of 1-(4-hexyloxy-2,2,6,6-tetramethylpiperidino)-2-phenyl-ethane-1,2-dione as a yellow oil (stabiliser 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04952620 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-5694b658392f45f6a07e629df628c163 |
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| Source note | uspto-grants-1990_08 |
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