HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1-(4-Phenyl-2-thiazolylmethyl)-4-phenylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(Chloromethyl)-4-phenyl-1,3-thiazole | HCID 22557361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Phenyl-2-thiazolylmethyl)-4-phenylpiperazine | HCID 22762508 | 75% |
Reaction Steps
A mixture of crude 2-chloromethyl-4-phenylthiazole (4.19g; 0.02 mole), N-phenylpiperazine (3.24 g; 0.02 mole) and finely-powdered, anhydrous sodium carbonate in absolute ethanol (60 ml) was stirred and boiled under reflux for 8 hours. The solvent was evaporated to dryness, solid residue suspended in water (100 ml) and then extracted with 2 × 100 ml CH2Cl2. The extracts were washed with water and dried over anhydrous MgSO4. On evaporation of the solvent, and recrystallisation of the residue from benzene/60°-80° C. petroleum ether mixture (with charcoal treatment) there was obtained the required product (5.03 g; 75%) having m.p. 142°-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04123529 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-163721578a66400cba94f5152a80b4bd |
| Source note | uspto-grants-1978_10 |