HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sebacoyl chloride → Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sebacoyl chloride | HCID 66072 | — |
| Reactant | 4-Piperidinol, 1,2,2,6,6-pentamethyl- | HCID 75472 | — |
| Reactant | 1,2,2,6,6-Pentamethylpiperidin-4-ol hydrochloride | HCID 20492522 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate | HCID 586744 | — |
Reaction Steps
A solution of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol in 50 parts of dry benzene was stirred at 15°-20° C. whilst adding 6.0 parts of sebacoyl chloride dropwise over 15 minutes. The mixture was stirred for a further 12 hours at room temperature after which the 1,2,2,6,6-pentamethylpiperidin-4-ol hydrochloride formed during the reaction was filtered off. The benzene was removed by distillation under reduced pressure to give a yellow oil, which was distilled under reduced pressure to give bis(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate as a colorless oil having a boiling point of 218°-20° C. at 0.4 mm of Hg and the following elemental analysis by weight:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049647 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-d6a1f4ccd52d4c7ab93b0288f2581946 |
| Source note | uspto-grants-1977_09 |