HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 101477-51-4
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | 2,3,4-Trimethoxybenzaldehyde | HCID 75006 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 1-[(4-fluorophenyl)(phenyl)methyl]piperazine | HCID 2778990 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 101477-51-4 | HCID 6447834 | 32.7% |
Reaction Steps
2,3,4-Trimethoxybenzaldehyde (7.85 g; 40.0 millimoles) and 10.8 g (39.9 millimoles) of 4-fluorobenzhydrylpiperazine (see German OLS 1929330) were melted in an oil bath at 120° C., and 2.3 ml (61.0 millimoles) of formic acid was added dropwise. The mixture was stirred under heat for 1 hour, and allowed to cool to room temperature. Then, 50 ml of an ethanol solution containing 5.0 g (43.1 millimoles) of fumaric acid was added, and the precipitated crystals were collected by filtration. Recrystallization of the crystals from ethanol gave 7.4 g (yield 32.7%) of 1-(2,3,4-trimethoxybenzyl)-4-(4-fluorobenzhydryl)piperazine fumarate as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04663325 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-88608b345fa54131849fc66348e05090 |
| Source note | uspto-grants-1987_05 |