Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Octanoyl chloride | HCID 8124 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 21505566 | HCID 21505566 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 21505572 | HCID 21505572 | — |
Reaction Steps
In accordance with the general procedure described in the foregoing Examples, 4.1 grams of 8-(n-butyl)-10-[4-(3-hydroxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin was reacted with 3.2 grams of caprylyl chloride (octanoyl chloride) in a mixture of 18 milliliters of benzene and 7 milliliters of chloroform. A solution of 2.3 grams of maleic acid in 25 milliliters of acetone was then added to the mixture and the resulting 8-(n-butyl)-10-[4-(3-oxtanoyloxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin di(hydrogen maleate) which had a melting point of 113°-115°C, after recrystallization from acetone, was recovered. Its elemental analysis corresponded to the empirical formula C41H56N2O10S. The free base was obtained in the form of a colorless very viscous oil which was very soluble in vegetable oils by dissolving the salt in a dilute aqueous ammonium hydroxide solution and extracting the solution with benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985750 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-6fa7f285c03c49d980b55938a59e805c |
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| Source note | uspto-grants-1976_10 |
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