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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1777360생성일: 2026년 10월 26일

1-Hydroxybenzotriazole hydrate → (4-(5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl)phenyl)methanol

https://huagongshe.com/reaction/1777360

반응식

참여 물질

역할이름HCID투입량
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물3-chloro-4-(2-methylpropyl)Benzoic acidHCID 59316720—
반응물HCID 178513316HCID 178513316—
용매DimethylformamideHCID 6228—
생성물(4-(5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl)phenyl)methanolHCID 70869326—

반응 조건

온도122.5 °C

반응 단계

N,N-Dicyclohexylcarbodiimide (1.07 g, 0.0052 mol) is added to a solution of 3-chloro-4-isobutylbenzoic acid (0.74 g, 0.0035 mol), N-hydroxy-4-hydroxymethylbenzamidine (0.867 g, 0.0052 mol) and N-hydroxybenzotriazole monohydrate (0.798 g, 0.0052 mol) in N,N-dimethylformamide (15 mL). The reaction mixture is heated at 120-125° C. for 2 hrs. It is then cooled to 0-5° C., filtered and washed with dichloromethane (2×20 mL). The filtrate is evaporated under reduced pressure and the residue is treated with demineralized water (20 mL). It is extracted with ethyl acetate (2×30 mL) and the combined extract is dried over sodium sulfate. Removal of solvent under reduced pressure gives a crude residue which is purified by column chromatography (silica gel 230-400, ethyl acetate:toluene, 15:85) to give {4-[5-(3-chloro-4-isobutylphenyl)-[1,2,4]-oxadiazol-3-yl]-phenyl}methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09266867B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-009c44ae601f4be8b37956c68656d75a
출처 메모uspto-grants-2016_02