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HRID 266605생성일: 2026년 10월 26일

Hydrochloric Acid → N-(4-t-butylphenyl)perylene-3,4-dicarboximide

https://huagongshe.com/reaction/266605

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ImidazoleHCID 795—
반응물4-Tert-ButylanilineHCID 69861—
반응물Perylene-3,4-dicarboxylic anhydrideHCID 11759069—
촉매Zinc acetate (USP)HCID 2724192—
용매EthanolHCID 702—
생성물N-(4-t-butylphenyl)perylene-3,4-dicarboximideHCID 1903322281.3%

반응 단계

0.70 g (2.17 mmol) of perylene-3,4-dicarboxylic anhydride is mixed with 0.49 g (3.28 mmol) of 4-t-butylaniline, 3.00 g of imidazole and 0.10 g of zinc acetate dihydrate and the mixture is heated at 140°-150° C. for 5 h. While still hot, the mixture is treated with 100 ml of ethanol, and then 200 ml of 10% hydrochloric acid are added. The red suspension is heated until all the ethanol has evaporated, and the product is then filtered off with suction. The red-brown residue is boiled in 10% potassium carbonate solution, the solid residue is filtered off with suction while hot and rinsed several times with hot dist. water. The red residue is dried in a drying cabinet at 120° C. and then recrystallized by extraction with a toluene/methanol mixture to give 0.80 g (81%) of red N-(4-t-butylphenyl)perylene-3,4-dicarboximide which shows a red solid fluorescence. M.p. >330° C. Rf (CHCl3 /silica gel)=0.35.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650513
출처 데이터셋uspto-grants-1997_07
ORD IDord-16dd334854764a0590178515dbeeb052
출처 메모uspto-grants-1997_07