HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Dibenz(c,e)oxepin-5(7H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphenic anhydride | HCID 72794 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dibenz(c,e)oxepin-5(7H)-one | HCID 4613402 | 75.7% |
Reaction Steps
9.0 g (0.24 mol) of sodium borohydride were added in portions at 5° C. in the course of 10 min to a suspension of 50.0 g (0.22 mol) of diphenic anhydride in 220 ml of DMF. After stirring at RT for 1 h, the reaction mixture was poured onto 220 ml of 6 M hydrochloric acid, diluted with 750 ml of water and stirred for 2 h. The deposited precipitate was filtered off with suction and 35.0 g of 7H-dibenzo[c,e]oxepin-5-one were obtained; m.p. 131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06686395B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-d2e8e7ec6a634f089861a868b6a4d799 |
| Source note | uspto-grants-2004_02 |