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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2359288생성일: 2026년 10월 25일

P-Cresol → 4-Methylphenyl 2,4,5-trifluorobenzoate

https://huagongshe.com/reaction/2359288

반응식

참여 물질

역할이름HCID투입량
반응물P-CresolHCID 2879—
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물2,4,5-Trifluorobenzoic acidHCID 521170—
용매DichloromethaneHCID 6344—
생성물4-Methylphenyl 2,4,5-trifluorobenzoateHCID 5804240866.4%

반응 조건

온도55 °C

반응 단계

Thionyl chloride (50 mL, 680 mmol) was added to 2,4,5-trifluorobenzoic acid (10 g, 57 mmol) and the mixture stirred at 55° C. for 18 hours. After cooling, the excess thionyl chloride was removed in vacuo. The resulting crude oil was azeotroped twice with DCM (30 mL) and toluene (20 mL) and the residue redissolved in DCM (50 mL), then cooled to 0° C. with an ice bath. A mixture of 4-methylphenol (6.4 g, 59 mmol) and triethylamine (10 mL, 71 mmol) in DCM (20 mL) was added over 30 minutes. The reaction was allowed to warm up to room temperature over 1 hour. The crude reaction mixture was partitioned between EtOAc (200 mL) and saturated sodium bicarbonate solution (70 mL). The aqueous layer was separated and extracted with EtOAc (100 mL). The combined organic extracts were combined, washed with saturated sodium bicarbonate solution (70 mL) and water (100 mL), dried over magnesium sulfate and concentrated in vacuo to provide a crude solid, which was purified by silica gel chromatography eluting with 5% EtOAc in heptane to provide the title compound (10.08 g, 66%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08685977B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-23bc6e40bbd346c4917fbb9d6c8a2ba8
출처 메모uspto-grants-2014_04