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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294674생성일: 2026년 10월 26일

Sodium Hydroxide → 2-{4,6-bis-[4-(2-Ethylhexyloxy)phenyl]-s-triazin-2-yl}-5-(2-ethylhexyloxy)phenol

https://huagongshe.com/reaction/2294674

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-Ethylhexyl bromideHCID 86804—
반응물4-{4,6-Bis[4-(2-ethylhexyloxy)phenyl]-s-triazin-2-yl}-1,3-dihydroxybenzeneHCID 135563262—
용매2-MethoxyethanolHCID 8019—
생성물2-{4,6-bis-[4-(2-Ethylhexyloxy)phenyl]-s-triazin-2-yl}-5-(2-ethylhexyloxy)phenolHCID 135576265101.5%

반응 단계

83.7 g (0.14 mol) of 4-{4,6-bis[4-(2-ethylhexyloxy)phenyl]-s-triazin-2-yl}-1,3-dihydroxy-benzene together with 500 ml of Methylcellosolve are placed at 80 C. in a 1 l sulfonating flask fitted with stirrer, condenser, internal thermometer and dropping funnel. 18.1 g of a 30% sodium hydroxide solution (0.16 mol) are added, the mixture is stirred for 15 minutes and then a solution of 31.4 g (0.16 mol) of 3-bromomethylheptane and 30 ml of Methylcellosolve are added dropwise over 30 minutes. After stirring at 110 C. for 24 hours, alkylation is complete (thin-layer chromatogram). The mixture is evaporated to dryness under vacuum, the residue is dissolved in 500 ml of toluene and filtered, and the filtrate is subjected to extraction by shaking with water. Drying of the extracts over sodium sulfate and removal of the solvent by distillation give 100.9 g of a red-brown oil. The crude product is dissolved in 200 ml of toluene/ethyl acetate (97.5/2.5) and, for purification, is chromatographed over silica gel (10 cm×40 cm), giving 79.4 g (80% of theory) of the compound of the formula ##STR26## as a honeylike red-brown resin.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05688995
출처 데이터셋uspto-grants-1997_11
ORD IDord-a68333c403a94aafa04345ba996afc9a
출처 메모uspto-grants-1997_11