HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 20343477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Phenol, 4-[(dimethylamino)methyl]-2,6-bis(1,1-dimethylethyl)- | HCID 66609 | — |
| Reactant | HCID 20343467 | HCID 20343467 | — |
| Reactant | Bis(1,2,2,6,6-pentamethylpiperidin-4-yl) propanedioate | HCID 20343478 | — |
| Product | HCID 20343477 | HCID 20343477 | — |
Reaction Steps
21.9 g (0.05 mole) of ethylmalonic acid-bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)ester, 20.5 g (0.05 mole) of malonic acid-bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)ester, 1.5 g (0.05 mole) of paraformaldehyde and 0.5 g of NaH are stirred in 120 ml of toluene for half an hour at room temperature and then for 7 hours at reflux temperature. After cooling, there is added 13.2 g (0.05 mole) of N-(3,5-di-tert.butyl-4-hydroxybenzyl)-dimethylamine, and the mixture is heated for 4 hours under reflux. Processing analogously to Example 1 yields 1-(3,5-di-tert.butyl-4-hydroxyphenyl)-2,2,4,4-tetra-(1,2,2,6,6-pentamethyl-4-piperidinyloxycarbonyl)-hexane as an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198334 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-79536e3b95fb44b097ab290b107767e1 |
| Source note | uspto-grants-1980_04 |