HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl bromide → 2-Bromomethyl-5-(3-trifluoromethylphenyl)-furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | {5-[3-(Trifluoromethyl)phenyl]furan-2-yl}methanol | HCID 7782745 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromomethyl-5-(3-trifluoromethylphenyl)-furan | HCID 22762571 | — |
Reaction Steps
The hydroxymethyl compound (4.84 g; 0.02 mole) prepared in (a) above, was dissolved in dimethylformamide (30 ml) cooled to 0°-5° C. and thionyl bromide (1.7 ml; 0.02 mole) was added dropwise with stirring. After 2 hours the greenish-yellow solution was poured onto ice/water and extracted via diethyl ether. The ether extract was washed with NaCl (saturated solution) dried over molecular sieve 3A and evaporated to give a light brown oil which slowly crystallised (4.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04123529 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-33ac89cf71744453914d7bc31feff290 |
| Source note | uspto-grants-1978_10 |