Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 66718671 | HCID 66718671 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68013273 | HCID 68013273 | — |
Reaction Steps
2.15 ml Benzoylchloride are dropwise added to a solution of 4.42 g 2,2,6,6-tetramethyl-1-phenyldiazenyl-piperidin-4-ol (see example 1) and 0.1 g 4-dimethylaminopyridine in 35 ml pyridine. The resulting mixture is stirred 4 hours at 23° C., then diluted with 300 ml ice-water. The precipitate is filtered off and recrystallized twice from methanol to afford 4.43 g of benzoic acid 2,2,6,6-tetramethyl-1-phenyldiazenyl-piperidin-4-yl ester as an off-white solid, m.p. 89-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940806B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-26f2452ffe564e1996a02dce91076a05 |
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| Source note | uspto-grants-2015_01 |
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