HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 19844666, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19844683 | HCID 19844683 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19844666 | HCID 19844666 | — |
Reaction Steps
To a mixture containing 10.6 g of 1-[2-[1-(2,5-dimethylphenyl)-1-phenylpropoxy]ethyl]piperazine and 4.6 g of anhydrous, powdered potassium carbonate in 90 ml of anhydrous benzene, 3.6 g of allyl bromide dissolved in 10 ml of benzene are dropped while mild refluxing, then the reaction mixture is boiled for one additional hour. After cooling down, water is added to the mixture, the organic phase is separated, washed with water until neutral, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The anhydrous ethanolic solution of the evaporation residue is treated with an ethanolic fumaric acid solution. The solid precipitate is recrystallized from methanol to give the aimed dihydrogen fumarate, m.p. 202°-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04874765 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-aa3b11f26b6d4db58de04161297c096c |
| Source note | uspto-grants-1989_10 |