HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Fluoro-3,4-dihydroxy-5-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Fluoro-3-hydroxy-5-nitro-p-anisonitrile | HCID 21459121 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-3,4-dihydroxy-5-nitrobenzonitrile | HCID 21458947 | — |
Reaction Steps
550 mg of 2-fluoro-3-hydroxy-5-nitro-p-anisonitrile are dissolved in 30 ml of methylene chloride, whereupon the solution is treated with 0.44 ml of boron tribromide. After stirring at 23° for 6 hours an additional 0.1 ml of boron tribromide are added thereto, whereupon the mixture is stirred at 23° for an additional 1.5 hours. Thereupon, ml of ethanol are added thereto at -15°. The reaction mixture is evaporated and the residue is dried in a high vacuum at 23°. By recrystallization from ether/hexane there is obtained 2-fluoro-3,4-dihydroxy-5-nitrobenzonitrile of m.p. 154°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476875 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-860b099832c94115bea5fb96aa40acb7 |
| Source note | uspto-grants-1995_12 |