HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxypiperidine → N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-3-hydroxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxypiperidine | HCID 23293 | — |
| Reactant | 3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acid | HCID 128570 | — |
| Product | N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-3-hydroxypiperidine | HCID 54203822 | 96% |
Reaction Steps
The procedure of Example 1 was repeated except that 6.1 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid and 3.0 g of 3-hydroxypiperidine were used as starting materials. 7.4 g (yield 96%) of the title compound was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04762829 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-82ff259194224e6ea0fbdfcd4bfde58e |
| Source note | uspto-grants-1988_08 |