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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 749261생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/749261

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Hydrochloric AcidHCID 313—
반응물p-ToluidineHCID 7813—
반응물Binap, (A+-)-HCID 634876—
반응물2-Bromo-1-chloro-3-fluorobenzeneHCID 21938660—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물(2-Chloro-6-fluorophenyl)-P-tolyl-amineHCID 21100364103.2%

반응 조건

온도110 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402603B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-3628d3297d5b49e9ac3bfa4c1c247357
출처 메모uspto-grants-2008_07