HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → tert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Boc-4-(4-Nitrobenzyl)piperazine | HCID 23506946 | — |
| Reactant | Tin tetrachloride dihydrate | HCID 85782573 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylate | HCID 12045001 | 89% |
Reaction Steps
4-(4-Nitro-benzyl)-piperazin-1-yl carboxylic acid tert-butyl ester (769 mg, 2.4 mmol) and tin chloride dihydrate (2.70 g, 12 mmol) are suspended in ethyl acetate (20 mL) and stirred at room temperature overnight. Then, saturated aqueous solution of sodium bicarbonate (20 mL) is added and vigorously stirred for 1 hour. Solids are removed by filtration and the organic layer of the filtrate is separated and washed with water (20 mL). The organic phase is dried over anhydrous magnesium sulfate and concentrated to give a white solid (620 mg, 89% yield, ES+(m/z) 293 [M+H]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767674B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-22a6201100424ded8c68ca25f011162c |
| Source note | uspto-grants-2010_08 |