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HRID 749261作成日:2026年10月25日

Methane → (2-Chloro-6-fluorophenyl)-P-tolyl-amine

https://huagongshe.com/reaction/749261

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Hydrochloric AcidHCID 313—
反応物p-ToluidineHCID 7813—
反応物Binap, (A+-)-HCID 634876—
反応物2-Bromo-1-chloro-3-fluorobenzeneHCID 21938660—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物(2-Chloro-6-fluorophenyl)-P-tolyl-amineHCID 21100364103.2%

反応条件

温度110 °C

反応手順

A mixture of 2-bromo-1-chloro-3-fluorobenzene (32 g, 153 mmol), p-toluidine (16.4 g, 153 mmol), sodium tert.butylate (27.5 g, 286 mmol), (±)-BINAP [2,2′-Bis-(diphenylphosphino)-1,1′-binaphthalin, 0.66 g, 1.1 mmol) and toluene (250 ml) is stirred under nitrogen for about 30 minutes. After the addition of Palladium-bis-(dibenzylidenaceton) (0.8 g, 1 mmol), the mixture is heated to 110° C. (slight reflux) for 14-20 hours. The mixture is then cooled to 30° C., water (60 ml), concentrated hydrochloric acid (60 ml) as well as charcoal and cellite (5 g each) are added and stirring is continued for an hour. The mixture is filtered and the filtrate is separated into the phases. The organic phase is washed with water (3 times, 70 ml each) and concentrated in vacuo to obtain 37.2 g of crude (2′-chloro-6′-fluorophenyl)-(4-methylphenyl)-amine. The product can be used in the next step (Step 1.2) as such; alternatively in can be kugelrohrdistilled in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07402603B2
出典データセットuspto-grants-2008_07
ORD IDord-3628d3297d5b49e9ac3bfa4c1c247357
出典メモuspto-grants-2008_07