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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1048생성일: 2026년 10월 23일

Dimethylformamide → 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl]-1H-tetrazole

https://huagongshe.com/ko/reaction/1048

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ammonium ChlorideHCID 25517—
반응물Sodium AzideHCID 33557—
반응물2-(2-Cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuranHCID 10155313—
용매WaterHCID 962—
생성물5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl]-1H-tetrazoleHCID 17841845178.1%

반응 단계

A mixture of 2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran (1.20 g), sodium azide (1.09 g), ammonium chloride (0.90 g) and N,N-dimethylformamide (30 ml) was stirred at 130° to 140° C. for 16 hours. The reaction mixture was poured over water and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with methanol-chloroform (5:95, v/v), 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole (1.05 g, 78%) was obtained, which was then recrystallized from dichloromethane-methanol to yield colorless prisms having a melting point of 177° to 178° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723479
출처 데이터셋uspto-grants-1998_03
ORD IDord-2e59b47848294fe195989e641f0b30fb
출처 메모uspto-grants-1998_03