HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824581Generated: October 26, 2026
O-Toluidine → 4-[1-(Bromo-difluoro-methyl)-1,2,2,2-tetrafluoro-ethyl]-2-methyl-phenylamine
https://huagongshe.com/reaction/1824581
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 1,2-Dibromo-1,1,2,3,3,3-hexafluoropropane | HCID 69579 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4-[1-(Bromo-difluoro-methyl)-1,2,2,2-tetrafluoro-ethyl]-2-methyl-phenylamine | HCID 10449644 | — |
Reaction Steps
First 154.36 g (0.887 mol) of sodium dithionite and then 50 g (0.467 mol) of o-toluidine (2-methylaniline) were added at room temperature to a mixture of 900 ml of water, 350 ml of tert-butyl methyl ether, 74.48 g (0.887 mol) of sodium hydrogencarbonate and 12.68 g of tetra-n-butylammonium hydrogensulphate. Subsequently, a solution of 274.684 g of 1,2-dibromo-1,1,2,3,3,3-hexafluoropropane in 100 ml of tert-butyl methyl ether was added dropwise at 35–40° C. and, on completion of addition, the mixture was stirred at 40° C. for a further 18 h. If necessary, sodium carbonate was used to adjust to a pH of 5 and the organic phase was removed, dried and concentrated. The remaining residue is incipiently distilled under reduced pressure at 0.3 mbar up to an internal temperature of 100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041852B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-d062f89ffb4a489990a2eedd0881b43c |
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| Source note | uspto-grants-2006_05 |
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