HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Methyl 3-(2,6-dichlorophenyl)-2-[3-[2-[[2-(tritylamino)ethoxy]methyl]phenyl]propanoyl]-2-propenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2,6-Dichlorobenzaldehyde | HCID 6737 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Methyl 3-oxo-5-[2-[[2-(tritylamino)ethoxy]methyl]phenyl]pentanoate | HCID 18765860 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl 3-(2,6-dichlorophenyl)-2-[3-[2-[[2-(tritylamino)ethoxy]methyl]phenyl]propanoyl]-2-propenoate | HCID 69684722 | — |
Reaction Steps
A mixture of methyl 3-oxo-5-[2-[[2-(tritylamino)ethoxy]methyl]phenyl]pentanoate (3.33 g, 6.38 mmol), 2,6-dichlorobenzaldehyde (1.12 g, 6.38 mmol), acetic acid (0.5 ml), piperidine (0.5 ml) and benzene (50 ml) was stirred for 4 hours at reflux temperature azeotropically. The reaction mixture was quenched with water (40 ml) and the whole was extracted with Et2O (20 ml×2). The combined extracts were washed with brine, dried over MgSO4, and concentrated in vacuo to afford the titled compound as a yellow oil. (quant.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06653313B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-fe88ccb6eb3348d79aef1ac1f7c21ae0 |
| Source note | uspto-grants-2003_11 |