HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20449623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 20449621 | HCID 20449621 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20449623 | HCID 20449623 | — |
Reaction Steps
10 g of 2,2,6,6-tetramethyl-4-[3,3-bis-(3-tert.-butyl-6-methyl-4-hydroxyphenyl)-propionyloxy]-piperidine are stirred in 25 ml of acetic anhydride at 110° for 6 hours. The acetic acid formed and excess anhydride are then distilled off under vacuum as completely as possible. The residue is cooled down to room temperature, 100 ml of water are added and are mixed in efficiently, and the precipitate is filtered off, is washed with water and is dried. Crystallising from acetonitrile gives 1-acetyl-2,2,6,6-tetramethyl-4-[3,3-bis-(3-tert.-butyl-6-methyl-4-hydroxyphenyl)-propionyloxy]-piperidine having a melting point of 270° (optical stabiliser No. 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04465765 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-745eeec8f5b3411995450ca670e9917f |
| Source note | uspto-grants-1984_08 |