HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 86734587, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| Product | HCID 86734587 | HCID 86734587 | — |
Reaction Steps
A mixture of 15.7 parts of 2,2,6,6-tetramethylpiperidin-4-ol and 8.3 parts of ethyl bromoacetate in 50 parts of ethyl alcohol was heated at reflux for 48 hours. The cooled reaction mixture was filtered to remove 2,2,6,6-tetramethylpiperidin-4-ol hydrobromide and the solvent removed by distillation in vacuo. The residue was triturated with 40°-60°C petroleum ether to remove the unreacted 2,2,6,6-tetramethylpiperidin-4-ol. The filtrate was then distilled under reduced pressure to yield pure 1-ethoxy-carbonylmethyl-2,2,6,6-tetramethylpiperidin-4-ol as a colourless liquid (of boiling point 116°C at 0.2 mm) which slowly solidified on standing (melting point 42°-42.5°C). This material gave the following elemental analysis by weight:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04014887 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-4649275a84894c0f8ace921b2342e252 |
| Source note | uspto-grants-1977_03 |