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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 743859생성일: 2026년 10월 26일

Hydrochloric Acid → 2,4-Bis(2,4-dihydroxy-5-hexylphenyl)-6-phenyl-s-triazine

https://huagongshe.com/reaction/743859

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물HexylresorcinolHCID 3610—
반응물2,4-Dichloro-6-phenyl-1,3,5-triazineHCID 15549—
반응물Aluminum(III) ChlorideHCID 6451240—
용매MethanolHCID 887—
용매WaterHCID 962—
용매SulfolaneHCID 31347—
생성물2,4-Bis(2,4-dihydroxy-5-hexylphenyl)-6-phenyl-s-triazineHCID 135843590—

반응 조건

온도80 °C

반응 단계

To a 750 mL sulfonation flask equipped with a mechanical stirrer, condenser, dropping funnel and a nitrogen atmosphere are charged 34.0 g (150 mmol) of 2,4-dichloro-6-phenyl-s-triazine, 44.0 g (330 mmol) of aluminum chloride and 100 mL of ligroin (boiling range 110°-140° C.). To that suspension, 60 mL of sulfolane are added dropwise with stirring over a 15 minute period with the temperature rising to 50° C. A solution of 62.1 g (320 mmol) of 4-hexylresorcinol in 60 mL of sulfolane is then added dropwise over a 15 minute period. The temperature rises to 60° C. and hydrogen chloride is evolved. The reaction mixture is heated to 80° C. for four hours. The lower layer of the two-phase mixture is poured into a solution of 50 mL of concentrated hydrochloric acid in 500 mL of methanol and 300 mL of water. The mixture is stirred at room temperature for 14 hours. The product obtained is suspended in 800 mL of water at 80° C. for 1 hour, is isolated by filtration and resuspended under the same conditions, finally isolated and dried at 85° C. under vacuum. The title compound is obtained as a crude orange product (77.0 g) and melts at 230°-238° C. It can be used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05556973
출처 데이터셋uspto-grants-1996_09
ORD IDord-1a6aaf4764c84b5a8532564f6474697f
출처 메모uspto-grants-1996_09