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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1025052생성일: 2026년 10월 25일

4-Hydroxybenzaldehyde → 4-(3,4,5-Tris-octadecyloxy-cyclohexylmethoxy)-benzaldehyde

https://huagongshe.com/reaction/1025052

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물TriphenylphosphineHCID 11776—
반응물3,4,5-Tris(octadecyloxy)cyclohexylmethyl alcoholHCID 86645785—
용매TetrahydrofuranHCID 8028—
생성물4-(3,4,5-Tris-octadecyloxy-cyclohexylmethoxy)-benzaldehydeHCID 59510354—

반응 단계

(3,4,5-Tris-octadecyloxy-cyclohexyl)-methanol (283 mg, 308 μmol), 4-hydroxy-benzaldehyde (56 mg, 459 μmol), and triphenylphosphine (121 mg, 461 μmol) were dissolved in dehydrated THF (5.5 mL), DIED (93.3 μL, 472 μmol) was added, and the mixture was stirred for 40 minutes. 4-Hydroxy-benzaldehyde, triphenylphosphine, and DIED (each 153 μmol) were added, and the mixture was stirred overnight. Triphenylphosphine and DIED (each 306 μmol) were added, and the mixture was stirred for 2.5 hours. THF was evaporated, and 90% aqueous acetonitrile (6 ml) was added to the residue to allow crystallization. The crystals were collected by filtration and thoroughly washed with acetonitrile to give crude crystals of 4-(3,4,5-tris-octadecyloxy-cyclohexylmethoxy)-benzaldehyde. The crude crystals were purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to give the object compound (130 mg, 127 μmol, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722934B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-98b714c752ea46cabaa827615c196a43
출처 메모uspto-grants-2014_05