HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl piperazine-1-carboxylate → Benzyl 4-(6-((tert-butyldimethylsily)oxy)hexyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl piperazine-1-carboxylate | HCID 643495 | — |
| Reactant | (6-Bromohexyloxy)-tert-butyldimethylsilane | HCID 4260352 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzyl 4-(6-((tert-butyldimethylsily)oxy)hexyl)piperazine-1-carboxylate | HCID 58505092 | 70% |
Reaction Steps
Intermediate 19 (2.6 g, 8.8 mmol) was added to a stirring solution of benzyl piperazine-1-carboxylate (1.1 mL, 5.87 mmol) in CH3CN (80 mL). The reaction mixture was refluxed over night, cooled, and quenched with satd. NaHCO3 (100 mL). The aqueous layer was extracted with EtOAc (3×50 mL) and the combined organic layers were washed with brine, dried over Na2SO4, concentrated to give the crude (3.8 g) as opaque oil. The chromatography (1:3, hexanes/EtOAc) afforded the title compound (1.78 g, 70%) as clear oil. ES/MS calcd. for C24H43N2O3Si+ 435.3. Found m/z=435.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394829B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-b7517b6ce9024bc09510a8896555697d |
| Source note | uspto-grants-2013_03 |