HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Trifluoromethyl)benzene → Benzene, 1-bromo-3-(trifluoromethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Trifluoromethyl)benzene | HCID 7368 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzene, 1-bromo-3-(trifluoromethyl)- | HCID 9817 | — |
Reaction Steps
3280 g of bromine are added to a mixture of 6046 g benzotrifluoride, 68 g FeCl3 and 2 g SiO2 at about 20° C. within ca. 2 hours. The reaction temperature is then slowly rised within ca. 7 hours to ca 40° C., 300 g water and 130 g Na2S2O3 are added and stirred for ca. 15 minutes. The phases are separated and the organic phase is destilled resulting in 4160 g bromo-benzotrifluoride (isomeric ratio 3:4=96:4) and 3290 g benzotrifluoride which is recycled.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420608B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-5ab084e949b34ab399eabe53e1dba916 |
| Source note | uspto-grants-2002_07 |