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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131664생성일: 2026년 10월 25일

4-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic Acid → 2'-Methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carbonyl chloride

https://huagongshe.com/reaction/131664

반응식

참여 물질

역할이름HCID투입량
반응물4-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic AcidHCID 11220119—
반응물2'-Methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carbonyl chloride Oxalyl chlorideHCID 86597648—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2'-Methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carbonyl chlorideHCID 21078801100%

반응 단계

2′-Methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carbonyl chloride Oxalyl chloride (0.073 ml, 0.82 mmol) was added to a suspension of 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxylic acid (200 mg, 0.68 mmol), and DMF (2 drops) in DCM (10 ml) at 0° C. The reaction was stirred at room temperature for 1.5 h and the solvents evaporated under vacuum to give 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carbonyl chloride as a white solid (0.212 g, 100%). NMR; δH [2H6]—DMSO 8.03,(2H, d), 7.90,(1H, dd), 7.76,(1H, d), 7.56-7.53,(3H, m), 2.56,(3H, s), 2.30,(3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384963B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-f33f4b1536534a2da71d49b19363aef9
출처 메모uspto-grants-2008_06