Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nordoxepin | HCID 4535 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 14677739 | HCID 14677739 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70389088 | HCID 70389088 | — |
Reaction Steps
To a stirred solution of 3-dibenz[b,e]oxepin-11(6H)-ylidene-N-methyl-1-propanamine (10.0 g, 0.033 mol) in DMF (80 mL) were added 6-bromo-1-[4-(1,1-dimethylethyl)phenyl]-1-hexanone (10.3 g, 0.033 mol) and potassium bicarbonate (6.6 g, 0.066 mol). The mixture was heated to 75°-80° C. under nitrogen for 28 hours. The reaction was cooled to ambient temperature, diluted with water (300 mL) and extracted with ethyl acetate (2×150 mL). The combined ethyl acetate extracts were washed with water (3×150 mL) and saturated NaCl (100 mL) and dried over magnesium sulfate. Removal of solvent gave an oil of 17.1 g. This oil was dissolved in 2-propanol (100 mL) and acidified with HCl gas. The solution was diluted to 400 mL with anhydrous ether and cooled. The solid was collected by filtration, recrystallized twice from ethyl acetate-methanol (15:1),and vacuum dried at 70° C. for 92 hours to provide 5.69 g of 3-dibenz[b,e]oxepin-11(6H)-ylidene-N-methyl-N-[6-[4-(1,1-dimethylethyl)phenyl]-6-oxohexyl]-1-propanamine hydrochloride, mp 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04855462 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-a1b3ba86160048b6aa7fd621ac5d67a7 |
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| Source note | uspto-grants-1989_08 |
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