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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1886498생성일: 2026년 10월 26일

Toluene → Methyl 4-(4-phenoxyphenoxy)benzoate

https://huagongshe.com/reaction/1886498

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Methyl 4-nitrobenzoateHCID 12083—
반응물2-Hydroxydiphenyl etherHCID 75491—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물Methyl 4-(4-phenoxyphenoxy)benzoateHCID 19876201—

반응 단계

Methyl 4-(4-phenoxyphenoxy)benzoate is synthesized as follows. A mixture of 15.00 g (80.6 mmoles) of -phenoxyphenol, 130 ml of N,N-dimethylformamide and 75 ml of toluene is agitated under nitrogen atmosphere. Potassium t-butoxide (9.32 g, 80.6 mmoles) is added with vigorous stirring and the mixture is heated to reflux. An azeotrope of t-butanol and toluene (85 ml) is collected at temperatures of 120° C. to 135° C. and is discarded. The mixture is cooled to ambient temperature, and a solution of 14.59 g (80.6 mmoles) of methyl 4-nitrobenzoate in 30 ml of N,N-dimethylformamide is added over a period of 15 minutes with cooling in a water bath. The mixture is heated at 100° C. for 14 hours, cooled to 20° C., and quenched with 1500 ml of ice water. The precipitate is filtered, dried in air and dissolved in 500 ml of acetone. The solution is filtered to remove insolubles, and the filtrate is concentrated by evaporation and cooled to precipitate methyl 4-(4-phenoxyphenoxy)benzoate. The recovered product weighs 1 23 g (82 percent yield) and has a melting point of 14° C. as determined by DSC.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05151489
출처 데이터셋uspto-grants-1992_09
ORD IDord-d56031083c1b4238a71fbafe1cac51d7
출처 메모uspto-grants-1992_09