HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Benzyl 1,4-diazepane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 1,4-diazepane-1-carboxylate | HCID 4384955 | 65.5% |
Reaction Steps
To 230 ml of dimethylformamide were added 25 g of homopiperazine and 5.4 g of sodium bicarbonate and then 25 ml of water followed by dropwise addition of 10 g of benzyloxycarbonyl chloride with stirring under ice cooling, and the mixture was stirred at a room temperature overnight. After evaporating off dimethylformamide under a reduced pressure, the reaction mixture was extracted three times with 100 ml of chloroform, and the extract was dried over magnesium sulfate and evaporated to remove the solvent under a reduced pressure. The resulting residue was applied to a silica gel column and eluted with chloroform/methanol (9:1), to obtain 9 g of the title compound as a light yellow liquor liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081246 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-987f173b83e74dee9822dfa8456064d4 |
| Source note | uspto-grants-1992_01 |