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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantSodium CarbonateHCID 10340—
ReactantSodium DithioniteHCID 24489—
Reactant1,2-Dibromo-1,1,2,3,3,3-hexafluoropropaneHCID 69579—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Product4-[1-(Bromo-difluoro-methyl)-1,2,2,2-tetrafluoro-ethyl]-2-methyl-phenylamineHCID 10449644—

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041852B2
Source datasetuspto-grants-2006_05
ORD IDord-d062f89ffb4a489990a2eedd0881b43c
Source noteuspto-grants-2006_05