HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → tert-Butyl 4-(2-ethoxy-2-oxoethyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Product | tert-Butyl 4-(2-ethoxy-2-oxoethyl)piperazine-1-carboxylate | HCID 22321826 | 68.2% |
Reaction Steps
Piperazine-1-carboxylic acid tert-butyl ester (2.62 g, 14 mmol), cesium carbonate (5 g, 15 mmol) and ethyl bromoacetate (1.56 ml, 14 mmol) was stirred at room temperature for 1 h. The mixture was partitioned between water (200 ml) and diethyl ether (2×100 ml). The combined organic phases were dried over magnesium sulphate and concentrated to give a yellow oil which crystallised to give 4-ethoxycarbonylmethyl-piperazine-1-carboxylic acid tert-butyl ester as a pale yellow solid (2.6 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612201B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-1c2b567b3df344e1afd591201709d5ae |
| Source note | uspto-grants-2009_11 |