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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477339생성일: 2026년 10월 24일

Ethanol → Ethyl (3-phenoxyphenyl)acetate

https://huagongshe.com/ko/reaction/477339

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sulfuric AcidHCID 1118—
반응물3-Phenoxyphenylacetic acidHCID 141749—
생성물Ethyl (3-phenoxyphenyl)acetateHCID 12509092—

반응 조건

온도20 °C

반응 단계

(3-Phenoxyphenyl)acetic acid (11.5 g) and 36N aqueous sulphuric acid solution (3 cc) in ethanol (200 cc) are brought to boiling for 72 hours. After being cooled to approximately 20° C., the reaction mixture is concentrated to dryness at 50° C. under reduced pressure (20 mm Hg; 2.7 kPa). The oil is dissolved in dichloromethane (300 cc); the organic phase is washed with water (150 cc), dried over anhydrous magnesium sulphate, filtered and concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue is dissolved in a mixture (20 cc) of cyclohexane and ethyl acetate (50:50 by volume), and the solution is poured onto silica (400 g) contained in a column 5 cm in diameter. Elution is performed with a mixture of cyclohexane and ethyl acetate (50:50 by volume), and the corresponding eluate is concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). Ethyl (3-phenoxyphenyl)acetate (7.4 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04886835
출처 데이터셋uspto-grants-1989_12
ORD IDord-70ed4016b51a42b78a92452f147dcbd8
출처 메모uspto-grants-1989_12