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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2413647생성일: 2026년 10월 27일

Ethylene Glycol → 10-(2-Hydroxyethoxy)-9-anthracenecarbaldehyde

https://huagongshe.com/reaction/2413647

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물NitrogenHCID 947—
반응물10-Chloro-9-anthraldehydeHCID 82703—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
생성물10-(2-Hydroxyethoxy)-9-anthracenecarbaldehydeHCID 13375405—

반응 단계

A 3 L 2-neck flask fitted with thermometer, condenser, stirring bar, N2 line and bubbler was charged with KOtBu (MCB, 25 g, 0.22 mol), 1,2-ethylene glycol (Fisher, 1.5 L) and 10-chloro-9-anthraldehyde (Aldrich, 50 g, 0.207 mol). The mixture was stirred at 100° for 1.5 h. An additional 5 g (45 mmol) of KOtBu was added and the stirring continued for an additional 0.5 h. The reaction mixture was cooled poured into cold H2O (1.5 L), then stirred for 10 min before the precipitate was collected by filtration. The yellow solid was dissolved in CH2Cl2 (1 L) and passed through a plug of SiO2 (100 g) using CH2Cl2 (9 L) as the eluting solvent. The CH2Cl2 contained impurities only and was discarded. The desired material was then eluted with EtOAc (12 L). The appropriate fractions were combined and the solvent removed to give (after drying at 50°) 28.82 g (53%), 10-(2-hydroxyethyloxy)-9-anthracenecarbaldehyde mp 142°-144°, (CH2Cl2 /hexane), (C, H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04719049
출처 데이터셋uspto-grants-1988_01
ORD IDord-45c430cce03747baa04aace19b1410ad
출처 메모uspto-grants-1988_01