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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 568335생성일: 2026년 10월 26일

Hydrochloric Acid → Dimethyl 4-phenoxyphthalate

https://huagongshe.com/reaction/568335

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,2-Benzenedicarboxylic acid, 4-nitro-, 1,2-dimethyl esterHCID 69119—
반응물Phenolate SodiumHCID 4445035—
용매DimethylformamideHCID 6228—
생성물Dimethyl 4-phenoxyphthalateHCID 19595677—

반응 단계

0.1 Mole of dimethyl 4-nitrophthalate and 0.1 mole of sodium phenolate were reacted with each other in a solvent of dimethylformamide at 100° C. over a 3-hour period under a stream of nitrogen. After being allowed to stand at room temperature and thereby cooled, the reaction mixture was poured into a dilute aqueous solution of hydrochloric acid, and extracted with ethyl acetate. The solvent was distilled away from the extract to yield dimethyl 4-phenoxyphthalate. Then, dimethyl 4-phenoxyphthalate thus-obtained was refluxed in a mixture of ethanol and an aqueous solution of potassium hydroxide to result in conversion into 4-phenoxyphthalic acid. Thereafter, the acid underwent reaction in an acetic acid/acetic anhydride mixture at a temperature of 100° C., and the solvent was distilled away from the reaction solution to yield 4-phenoxyphthalic anhydride. Subsequently, equimolar amounts of 4-phenoxyphthalic anhydride. Subsequently, equimolar amounts of 4-phenoxyphthalic anhydride and m-diethylaminophenol were refluxed in toluene to yield a 2-(2-hydroxy-4-diethylaminobenzoyl)-4- or -5-aryloxybenzoic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04728633
출처 데이터셋uspto-grants-1988_03
ORD IDord-67aea6715aa24828bb278aa9828acc6a
출처 메모uspto-grants-1988_03