HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,5-Dibenzyl-2,5-diazabicyclo[2.2.2]octane-3,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,5-Diazabicyclo[2.2.2]octane-3,6-dione | HCID 12853591 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,5-Dibenzyl-2,5-diazabicyclo[2.2.2]octane-3,6-dione | HCID 21545490 | 91.7% |
Reaction Steps
A hot solution of 36.6 g (0.262 mole) of 2,5-diazabicyclo[2.2.2]octane-3,6-dione in 800 ml dry dimethylformamide was added rapidly from a dropping funnel to 12.5 g (0.52 mole) of oil-free sodium hydride. After stirring for 1 hour, the mixture was chilled and treated with 67.5 ml (0.59 mole) benzyl chloride during a period of a few minutes. After stirring at room temperature for 18 hours, 1 liter of water was added cautiously, and the mixture was extracted with chloroform. The extracts were washed with water, dried with sodium sulfate, and evaporated to dryness to yield a crystalline residue. Trituration in diethyl ether provided 77.0 g (91%) of product as colorless needles, melting point 168°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03951980 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-49690161c74641e48de5bed8844c4c7c |
| Source note | uspto-grants-1976_04 |