HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → HCID 54346849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 69972355 | HCID 69972355 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54346849 | HCID 54346849 | 102.1% |
Reaction Steps
To a solution of (2R)-4-methanesulfonylpiperazine-2-carboxylic acid hydrochloride (2.10 g) in H2O (20 ml) and dioxane (20 ml) were added NaHCO3 (2.38 g) and a solution of benzyloxycarbonyl chloride (1.76 g) in Et2O (10 ml) at room temperature. After stirring for 2 hours, Et2O and dioxane were evaporated in vacuo. The solution was acidified with 1N HCl and extracted with AcOEt (80 ml). The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo to give 3.0 g of (2R)-1-benzyloxycarbonyl-4-methanesulfonylpiperazine-2-carboxylic acid as an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06333324B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-16d1cc937b98422994b5dae3817b6c50 |
| Source note | uspto-grants-2001_12 |