HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → p-Formylphenyl 1-amidino-4-piperidinepropionate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Amidino-4-piperidinepropionic acid hydrochloride | HCID 15583512 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | p-Formylphenyl 1-amidino-4-piperidinepropionate hydrochloride | HCID 86739279 | 36.4% |
Reaction Steps
A mixture of 4.0 g of 1-amidino-4-piperidinepropionic acid hydrochloride and 2.1 g of p-hydroxybenzaldehyde was suspended in 20 ml of dry pyridine. 3.5 g of dicyclohexylcarbodiimide was added with stirring to the suspension, and the resulting mixture was stirred overnight at room temperature. After removal of any insoluble materials, the filtrate was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was stirred to give crystals. The crystals were recrystallized from methanol-ether to obtain 2.1 g (yield: 36.4%) of p-formylphenyl 1-amidino-4-piperidinepropionate hydrochloride as colorless crystals having a melting point of 144° to 147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04433152 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-5af6023b70d844b9b134f63e8d5cff30 |
| Source note | uspto-grants-1984_02 |