HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 8-Chloro-6,11-dihydro-5H-dibenz[b,e]azepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13364646 | HCID 13364646 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Chloro-6,11-dihydro-5H-dibenz[b,e]azepine | HCID 13364647 | — |
Reaction Steps
To a suspension of 1.5 g lithium aluminium hydride in 100 ml tetrahydrofuran is added with ice cooling first 1.05 ml chloroform and thereafter portionwise 3.0 g of 8-chloro-5,6-dihydro-11H-dibenz[b,e]azepin-6-one. The mixture is stirred at room temperature for 15 hours. To the mixture is then added dropwise under ice cooling 9.0 ml of a saturated solution of potassium carbonate. The precipitate is filtered off and washed with ether. The filtrate is then evaporated and the residue recrystallised from methylene chloride/ether/petroleum ether to give the heading compound, m.p. 132°-135°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04434171 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-af8ac39ac91b458b935988b3f9619988 |
| Source note | uspto-grants-1984_02 |