Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | HCID 12838118 | HCID 12838118 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12838137 | HCID 12838137 | 54% |
Reaction Steps
A mixture of 20 g of 1-{3-[4-(3-methoxycarbonyl-propionamido)-2-methoxyphenoxy]-n-propyl}-4-phenyl-piperazine and 2 ml of xylene is stirred at 150° C. for 20 hours. Then, chloroform is added to the reaction mixture, and said mixture is treated with activated charcoal and then evaporated under reduced pressure to remove the solvent. The residue is purified by silica gel chromatography (Solvent: 1% methanol/chloroform), and then recrystallized from ethyl acetate. 910 mg of 1-[3-(4-succinimido-2-methoxyphenoxy)-n-propyl]-4-phenyl-piperazine are obtained as colorless needles. Yield: 54%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04413006 |
|---|
| Source dataset | uspto-grants-1983_11 |
|---|
| ORD ID | ord-7c2c6f3cb8fd44d7824bb1cafc30d6a5 |
|---|
| Source note | uspto-grants-1983_11 |
|---|