HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Cyclopentyloxy-4-methoxybenzal hydantoin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Cyclopentyloxy-4-methoxybenzaldehyde | HCID 2735893 | — |
| Reactant | Diethyl 5-hydantoylphosphonate | HCID 3516088 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Cyclopentyloxy-4-methoxybenzal hydantoin | HCID 54350727 | 77.8% |
Reaction Steps
To a stirred solution of diethyl 5-hydantoylphosphonate (10 g, 42.3 mmol) and triethylamine (5.70 g, 56 mmol), in dry acetonitrile (100 ml), at room temperature was added a solution of 3-cyclopentyloxy-4-methoxybenzaldehyde (8 g, 36.3 mmol) in dry acetonitrile (75 ml), dropwise over 30 minutes. The resulting mixture was stirred at room temperature overnight, after which volatiles were removed in vacuo. The residue was diluted with 0.05N HCl (120 ml) and the precipitate collected by filtration. Recrystallization of this material with methylene chloride/methanol/diethyl ether afforded the title compound as a pale yellow solid (8.54 g), m.p. 220-222° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248769B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-45b0bca773284945b314b1cf571bdcad |
| Source note | uspto-grants-2001_06 |