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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1784331생성일: 2026년 10월 24일

Phthalic Anhydride → 2-(2,4-Dihydroxy-3-methylbenzoyl)benzoic acid

https://huagongshe.com/ko/reaction/1784331

반응식

참여 물질

역할이름HCID투입량
반응물Phthalic AnhydrideHCID 6811—
반응물2-MethylresorcinolHCID 11843—
반응물Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
용매1,1,1,2-TetrachloroethaneHCID 12418—
생성물2-(2,4-Dihydroxy-3-methylbenzoyl)benzoic acidHCID 21083111—

반응 단계

Aluminum chloride (21.4 g, 161 mmol) was added to a stirring suspension of phthalic anhydride (6 g, 40 mmol) in tetrachloroethane (200 mL) under nitrogen. 1,3-Dihydroxy-2-methylbenzene (5 g, 40 mmol) was added and the mixture quickly thickened. After the precipitates were broken up with a spatula the reaction continued for 1 hour. The solution was diluted with ethyl acetate (˜600 mL) and washed with 1 M hydrochloric acid (2×200 mL). The product was extracted from the organic layer into a saturated solution of sodium bicarbonate in water (600 mL). The basic aqueous phase was acidified with 3M hydrochloric acid to a pH of 5. The product was extracted from the aqueous phase into ethyl acetate (400 mL), washed with brine (2×100 mL), dried over magnesium sulfate and concentrated to give a brownish solid. The solid was slurried in dichloromethane (20 mL) and filtered to give 2-(2,4-dihydroxy-3-methylbenzoyl)benzoic acid as an off white powder (4.6 g, 16.9 mmol, 42% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07504360B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-4d55731c11f64cea9f07bcf59e7d1826
출처 메모uspto-grants-2009_03