Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(2-Chloroethyl)-4-(2-methoxyphenyl)piperazine | HCID 595673 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 19972356 | HCID 19972356 | 50.6% |
Reaction Steps
A mixture of 6.73 g of N-hydroxyphthalimide, 3.73 g of sodium acetate and 10 g of 1-(2-chloroethyl)-4-(2-methoxyphenyl)piperazine in 100 ml of anhydrous dimethylsulfoxide was stirred at 100° C. for 4 hours. The reaction mixture was then cooled to room temperature, poured into water and extracted with ethyl acetate. The collected organic layers were washed with 1N sodium hydroxide, dried on anhydrous sodium sulfate and evaporated to dryness in vacuo to give 7.58 g of the title compound. A sample was crystallized from cyclohexane, m.p. (76) 80°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403842 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-6064556696b946bc8e92a010a8862b2a |
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| Source note | uspto-grants-1995_04 |
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