HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diiodomethane → 1-tert-Butoxycarbonyl-2(S)-(2-cyclopropyloxyethyl)-4-(1-naphthoyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | 1-tert-Butoxycarbonyl-2(S)-(2-vinyloxyethyl)-4-naphthoylpiperazine | HCID 22884137 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-tert-Butoxycarbonyl-2(S)-(2-cyclopropyloxyethyl)-4-(1-naphthoyl)piperazine | HCID 22884129 | — |
Reaction Steps
1-tert-Butoxycarbonyl-2(S)-(2-vinyloxyethyl)-4-naphthoylpiperazine (0.107 g, 0.261 mmol) was dissolved in ether (5 mL) under an argon atmosphere. To this solution was added diiodomethane (0.042 mL, 0.522 mmol) and diethylzinc (0.39 mL, 1M in hexane, 0.39 mmol). The reaction was refluxed for 1 h. The reaction was quenched with water, and extracted with ethyl acetate. The organic extracts were washed with water, saturated sodium chloride, and dried over magnesium sulfate. The title compound was obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05736539 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-a4d12b23dec64b89912942c36fdbdeac |
| Source note | uspto-grants-1998_04 |