HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815610Generated: October 26, 2026
Decalin → 5-(4-(2-hydroxyethyl)phenyl)-5H-dibenz[b,f]azepine
https://huagongshe.com/reaction/1815610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Decalin | HCID 7044 | — |
| Reactant | Dibenz(b,f)azepine | HCID 9212 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(4-Iodophenyl)ethan-1-ol | HCID 3040770 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-(4-(2-hydroxyethyl)phenyl)-5H-dibenz[b,f]azepine | HCID 13008248 | 30% |
Reaction Steps
A mixture of 8.7 g (45 mmol) of 5H-dibenz[b,f]azepine, 12.4 g (50 mmol) of p-iodophenethyl alcohol, 2.8 g (50 mmol) of potassium hydroxide, 4. 8 g (75 mmol) of copper powder, and 20 ml of decalin was heated at an external temperature of 200° C. while stirring in a nitrogen stream for 40 hours. The reaction mixture was cooled nearly to room temperature, chloroform was added thereto, followed by filtration using Celite to remove any insoluble matter. The filtrate was concentrated. To remove decalin, n-hexane was added to the residue, followed by filtration. The filter cake was reprecipitated in methanol, and the resulting crude product was purified by silica gel column chromatography to give 4.2 g (30%) of 5-(4-(2-hydroxyethyl)phenyl)-5H-dibenz[b,f]azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878822B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-6f51176524f446d89081b4557b98c0a5 |
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| Source note | uspto-grants-2005_04 |
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