HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287616Generated: October 29, 2026
Dodecanoyl chloride → HCID 21505557, compound
https://huagongshe.com/reaction/1287616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | HCID 114710 | HCID 114710 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 21505557 | HCID 21505557 | — |
Reaction Steps
In accordance with the general method described in the foregoing Examples, 10.15 grams of 8-ethyl-10-[4-(3-hydroxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin was reacted with a solution of 12.5 grams of lauroyl chloride (dodecanoyl chloride) in a mixture of 60 milliliters of benzene and 20 milliliters of chloroform. By adding a solution of 6.15 grams of maleic acid in 60 milliliters of acetone to the crude product, 14.0 grams of 8-ethyl-10-[4-(3-dodecanoyloxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin di(hydrogen maleate) was recovered. The salt, after recrystallization from acetone, had a melting point of 126°-128°C. Its elemental analysis corresponded to the empirical formula C43H60N2O10S. 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 resulting 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-f0ba1e7c01aa4b7aad538a650eb960ba |
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| Source note | uspto-grants-1976_10 |
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