HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 4[((tert-butoxycarbonyl)[2-[(5-phenylpentyl)oxy]-phenethyl]amino)-methyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (5-Bromopentyl)benzene | HCID 285561 | — |
| Reactant | Methyl 4-{[(tert-butoxycarbonyl)-(2-hydroxyphenethyl)-amino]methyl}benzoate | HCID 22014997 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4[((tert-butoxycarbonyl)[2-[(5-phenylpentyl)oxy]-phenethyl]amino)-methyl]benzoate | HCID 22015039 | — |
Reaction Steps
1.78 g (4.63 mmol) of methyl 4-{[(tert-butoxycarbonyl)-(2-hydroxyphenethyl)-amino]methyl}benzoate from Ex.V.2, 1.05 g (4.63 mmol) of 5-phenyl-1-bromopentane and 0.77 g (5.55 mmol) of potassium carbonate in 15 ml of acetonitrile are heated at reflux for 18 hours. The reaction mixture is poured into water, extracted with ethyl acetate and dried over magnesium sulphate and the solvent is distilled off under reduced pressure. A solid is obtained which is reacted further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517896B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-075d8e8e2eb54ca1a537d49746db75a6 |
| Source note | uspto-grants-2009_04 |