HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-4-fluorobenzene → 2-(3,5-Dichloro-4'-fluoro-2-[1,1'-biphenyl]yl)-4,4-dimethyl-2-oxazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-(2,4-Dichloro-6-methoxyphenyl)-4,4-dimethyl-2-oxazoline | HCID 12802883 | — |
| Reactant | HCID 178418676 | HCID 178418676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3,5-Dichloro-4'-fluoro-2-[1,1'-biphenyl]yl)-4,4-dimethyl-2-oxazoline | HCID 12802884 | 85% |
Reaction Steps
4-Fluorophenylmagnesium bromide, prepared from 4-fluorobromobenzene (120 mmol) and magnesium (120 mmol), in dry THF (75 ml) was added dropwise to a stirred solution of 2-(2,4-dichloro-6-methoxyphenyl)-4,4-dimethyl-2-oxazoline (100 mmol) in dry THF (150 ml) under N2 at 20° C. Stirring of the solution was continued for 20 hours and then the reaction mixture was quenched by the addition of saturated ammonium chloride solution. The resulting mixture was extracted with ether (2×500 ml), dried over MgSO4, filtered and evaporated. The residue was chromatographed on silica gel (ethyl acetatehexane) to provide title compound (85%), mp 93°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04308378 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-6a1e8ca51f7e41bf8b9aee9bd0401a08 |
| Source note | uspto-grants-1981_12 |