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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1702504생성일: 2026년 10월 24일

Phthalic Acid → Diprop-2-en-1-yl 3,4,5,6-tetrachlorobenzene-1,2-dicarboxylate

https://huagongshe.com/ko/reaction/1702504

반응식

참여 물질

역할이름HCID투입량
반응물Phthalic AcidHCID 1017—
반응물Allyl chlorideHCID 7850—
반응물Diallyl phthalateHCID 8560—
반응물Disodium tetrachlorophthalateHCID 20504075—
생성물Diprop-2-en-1-yl 3,4,5,6-tetrachlorobenzene-1,2-dicarboxylateHCID 22450728—

반응 단계

Using a method similar to the known preparation of diallyl phthalate by reacting allyl chloride with metal salts of phthalic acid, Matsumoto et al prepared DATCP by reacting disodium tetrachlorophthalate with 2 moles of allyl chloride in an aqueous solution containing cuprous ions. Diallyl tetrachlorophthalate was also produced by Guseinov et al who reacted the anhydride with 3 moles of allyl alcohol plus 1 mole of hydrochloric acid in a benzene solution (Azerbaizhan Chemical Journal, No. 6, (1964), 21-23). Nordlander et al also produced DATCP by reacting the tetrachlorophthalic anhydride with 2 moles of allyl alcohol using sulfuric acid as a catalyst and driving off the water of reaction by distillation as an azeotrope with benzene (Journal of the American Chemical Society, 69, Nov., (1947), 2679-2682). However, only a 10% to 15% yield of the DATCP was obtained because of dehydration and polymerization reactions of the allyl alcohol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04381406
출처 데이터셋uspto-grants-1983_04
ORD IDord-9e0fc8d2fa924861befa2fd30dd70fbd
출처 메모uspto-grants-1983_04