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HRID 1824581作成日:2026年10月27日

O-Toluidine → 4-[1-(Bromo-difluoro-methyl)-1,2,2,2-tetrafluoro-ethyl]-2-methyl-phenylamine

https://huagongshe.com/reaction/1824581

反応式

関与物質

役割名称HCID仕込み量
反応物O-ToluidineHCID 7242—
反応物Sodium CarbonateHCID 10340—
反応物Sodium DithioniteHCID 24489—
反応物1,2-Dibromo-1,1,2,3,3,3-hexafluoropropaneHCID 69579—
反応物Sodium BicarbonateHCID 516892—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒WaterHCID 962—
溶媒tert-Butyl methyl etherHCID 15413—
生成物4-[1-(Bromo-difluoro-methyl)-1,2,2,2-tetrafluoro-ethyl]-2-methyl-phenylamineHCID 10449644—

反応条件

温度40 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07041852B2
出典データセットuspto-grants-2006_05
ORD IDord-d062f89ffb4a489990a2eedd0881b43c
出典メモuspto-grants-2006_05