Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | 10-Methoxyiminostilbene | HCID 78424 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54152167 | HCID 54152167 | 92.8% |
Reaction Steps
A 500 ml round bottom flask containing 9.87 g (0.044 moles) of 10-methoxy-5H-dibenz[b,f]azepine prepared in Example 3 and 13.9 g (0.088 moles) of 3-dimethylaminopropylchloride was evacuated for several days. Anhydrous toluene (250 ml) was added followed by 7.04 g (0.176 moles) of sodium amide. The heterogeneous solution was stirred at ambient temperature for a few minutes and then refluxed for 16 hours. After 16 hours of refluxing, tlc analysis of the reaction mixture (silica gel GF plates, methanol:chloroform 1:9; visualized under UV lamp and sulfuric acid-ceric sulfate spray) revealed that the reaction was complete and that no starting material remained. Enough water was added to slowly decompose the excess sodium amide. The dark-brown solution was placed in a 1 liter separatory funnel and extracted with four 250 ml portions of water. The organic phase was dried over anhydrous magnesium sulfate, charcoal was added and the mixture was filtered through a Celite pad. The filtrate was concentrated leaving a brown oil (12.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04275160 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-bc3a464ce9fd443190c8cb4d5e8e98ca |
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| Source note | uspto-grants-1981_06 |
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