HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-yl)ethyl carbanilate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | 2-(6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-yl)ethanol | HCID 13457012 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-yl)ethyl carbanilate | HCID 13457011 | 67.8% |
Reaction Steps
A stirred solution of 2.54 g (0.01 mol) of 2-(6,11-dihydro-11-oxodibenz[b,e]oxepin-2-yl)ethanol of Example 1, 20 ml of sieve dried CH2Cl2 and 1.55 g (0.013 mol) of phenylisocyanate was heated 20 hours under reflux with exclusion of moisture. The cooled solution was concentrated on a rotary evaporator to afford an oil which was dissolved in 10 ml of hot toluene. The solution was seeded with product (previously obtained by the method described herein), stirred until a thick suspension formed and allowed to stand overnight (about 16 hours) at ambient temperature. Filtration and drying in vacuo afforded 2.53 g (67.8%) of a colorless solid of 2-(6,11-dihydro-11-oxodibenz[b,e]oxepin-2-yl)ethyl carbanilate, m.p. 98°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576960 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-42041ab3a8bb46119e05d4e41355e293 |
| Source note | uspto-grants-1986_03 |