HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → N-Cyclohexyl-N-(2,2,6,6-tetramethyl-4-piperidinyl)formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | ST038767 | HCID 729174 | — |
| Catalyst | Tetrabutoxytitanium | HCID 521701 | — |
| Product | N-Cyclohexyl-N-(2,2,6,6-tetramethyl-4-piperidinyl)formamide | HCID 14419060 | — |
Reaction Steps
80 g of 4-(N-cyclohexylamino)-2,2,6,6-tetramethylpiperidine and 32 g of tetrabutyl orthotitanate in 175 ml of ethyl formate were refluxed for 11 hours. Fractional distillation gave a fraction of boiling point 143°-144° C. under 0.4 mmHg. After solidification, this fraction was recrystallized from n-hexane. 4-(N-cyclohexyl-N-formylamino)-2,2,6,6-tetramethylpiperidine was isolated as a colorless solid of melting point 105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04976889 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-5b7b836826304f49898d9f28caa364e8 |
| Source note | uspto-grants-1990_12 |