HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20133425, compound → 6-Fluoro-2H-1,4-benzoxazin-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20133425 | HCID 20133425 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Fluoro-2H-1,4-benzoxazin-3(4H)-one | HCID 302897 | 88.6% |
Reaction Steps
A solution of 46 g of ethyl 4-fluoro-2-nitrophenoxyacetate, prepared in Example 18, in 500 ml of methanol is hydrogenated under atmospheric pressure in the presence of Raney nickel. After absorption of the theoretical quantity of hydrogen, the catalyst is filtered off, the solution is concentrated in vacuo and the residue is taken up in either, from which it crystallizes. The crystals formed are filtered off, washed with ether and dried. 28 g of 6-fluoro-2H-1,4-benzoxazin-3(4H)-one are thus obtained in the form of crystals of melting point 206°-207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755509 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-5143396895a348108eed13b8051e5381 |
| Source note | uspto-grants-1988_07 |