Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21564445 | HCID 21564445 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21564443 | HCID 21564443 | — |
Reaction Steps
A mixture of 100 mg of 3,4-dimethoxy-10-hydroxy-5,6,7,8,13,14-hexahydrodibenz[c,g]azecine, 42.6 ml of allyl bromide and 32.3 mg of sodium bicarbonate in 4 ml of dimethylformaide is stirred for 2 hours at 100°C in argon atmosphere. After cooling, 40 ml of water is added to the mixture, and the mixture is extracted with methylene chloride. The extract is washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure. The residue is dissolved in benzene, passed through a column of 3.8 g of silica gel, and eluated with benzene - ethyl acetate (10 : 1). The evaporation of the solvent affords 106 mg of 6-allyl-3,4-dimethoxy-10-hydroxy-5,6,7,8,13,14-hexahydrodibenz[c,g]azecine as a colorless oily material. IR: νmaxCHCl 3 3604, 3420 and 1641 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03932384 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-17b56aee5c154944a38e59d5e40501f9 |
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| Source note | uspto-grants-1976_01 |
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