Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(2-Ethoxyphenoxy)ethylamine | HCID 5303042 | — |
| Reactant | HCID 21496613 | HCID 21496613 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21496591 | HCID 21496591 | — |
Reaction Steps
A mixture of 4.4 g of 4-ethoxy-4-(4-fluorophenyl)-butyl chloride, 3.6 g of 2-(2-ethoxyphenoxy)ethylamine, 2 g of sodium bicarbonate and 44 ml of N,N-dimethylformamide was stirred at about 110° C for 20 hours. After cooling, the reaction mixture was poured into cold water and extracted with benzene. The benzene layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The oily residue was treated with ethanolic oxalic acid and recrystallized from ethanol to give N-[4-ethoxy-4-(4-fluorophenyl)butyl]-2-(2-ethoxyphenoxy)-ethylamine oxalate, M.P. 157° - 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03993780 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-b06bd60d568b4661af8b5941a6d78a76 |
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| Source note | uspto-grants-1976_11 |
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