HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(Anilinomethylidene)-1-benzoxepine-3,5(2H,4H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 178519899 | HCID 178519899 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(Anilinomethylidene)-1-benzoxepine-3,5(2H,4H)-dione | HCID 53962065 | 58% |
Reaction Steps
A quantity of 10.0g (0.049 mole) of 2,3-dihydro-5-hydroxy-3-oxo-1-benzoxepin-4-carboxaldehyde was added to 15g of aniline. The temperatuure rose to 45° as most solid went into solution. The dark mixture was heated at 105°-110° for 10 minutes and cooled. Ether (500ml) and 300ml of cold 2N hydrochloric acid were added, and the mixture was stirred for 5 minutes. The entire mixture was filtered to remove the dark, suspended insolubles. The ether phase of the filtrate was washed well with water, dried (Na2SO4) and concentrated to give 8.0g (58%) of crude product; m.p. 94°-96°. Recrystallization from ethyl acetate gave pure, orange-tan crystals; m.p. 98°-100°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04001224 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-aa96c04062594e83bc5a8efc665a1988 |
| Source note | uspto-grants-1977_01 |