HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 68561168, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N,N-diethyl-2-(3-formyl-1H-indol-1-yl)acetamide | HCID 820167 | — |
| Reactant | 2,3-dihydro-1H-indolizinium chloride | HCID 68563060 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 68561168 | HCID 68561168 | — |
Reaction Steps
0.800 g of N,N-diethyl-2-(3-formyl-1H-indol-1-yl)acetamide was solubilized in 4.2 ml of isopropanol. 0.238 g of piperidine was added, followed by 0.435 g of 2,3-dihydro-1H-indolizinium chloride dissolved in 7 ml of isopropanol. The reaction mixtures were brought to 80° C. for 24 h, with stirring. 50 ml of ethyl acetate were added in order to precipitate the dye. The precipitate was filtered off, and washed with 3 times with 25 ml of ethyl acetate before being dried under vacuum until a constant weight was obtained. 1.09 g of orange powder were recovered. The analyses were in conformity with the expected structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07744658B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-e3890998a6f74fe4bce322bc689e3077 |
| Source note | uspto-grants-2010_06 |