돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219773생성일: 2026년 10월 26일

Water → Methyl 2-methyl-2'-(trifluoromethyl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/219773

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2-(Trifluoromethyl)benzeneboronic acidHCID 2734387—
반응물Methyl 4-bromo-3-methylbenzoateHCID 3294148—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물Methyl 2-methyl-2'-(trifluoromethyl)biphenyl-4-carboxylateHCID 5960653996%

반응 단계

Methyl 4-bromo-3-methylbenzoate (ABCR. 3 g; 13.10 mmol; 1 eq.), 2-(trifluoromethyl)phenylboronic acid (2.736 g; 14.41 mmol; 1.10 eq.), potassium carbonate (9.049 g; 65.48 mmol; 5 eq.), tetrakis(triphenylphosphine)palladium(0) (1.51 g; 1.31 mmol; 0.10 eq.) were mixed in Toluene (15 mL) and water (15 mL) under N2 atmosphere. The reaction mixture was degassed with N2 for 10 min and was heated under reflux for 3 hours. The reaction mixture was cooled to RT, filtered over a pad of celite and washed with toluene (500 mL). The filtrate was concentrated under vacuum to afford brown oil. It was taken in EtOAc (500 mL). The organic layer was washed with a saturated aqueous solution of NaHCO3 (200 mL), water (200 mL) and brine (200 mL). It was dried over MgSO4, filtered off and concentrated under vacuum giving a brown oil (3.7 g, 96%). It was used in the next step without further purification. LC/MS (Method A): 294.5 (M+H)+. HPLC (Method A) Rt 5.34 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202865B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-dd014a3b3da744b9b642a23ff1eb1ad4
출처 메모uspto-grants-2012_06