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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1377831생성일: 2026년 10월 27일

Triphenylphosphine → 5-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furan

https://huagongshe.com/reaction/1377831

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Win 58768HCID 148372—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물5-Ethyl-2-(3-hydroxypropyl)furanHCID 22915401—
용매WaterHCID 962—
생성물5-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furanHCID 1595464365.4%

반응 단계

Diethyl azodicarboxylate (DEAD, 4.84 g; 27.8 mmol) was added under nitrogen to a stirred and cooled (-20° C.) solution of triphenylphosphine (7.37 g; 27.8 mmol), 5-ethyl-2-(3-hydroxypropyl)furan (Intermediate 1c) (3.9 g; 25.3 mmol), and 4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenol (5.69 g; 27.8 mmol). The mixture was stirred at -20° C. for 1/2 h, and then was allowed to warm to room temperature overnight. Water (50 mL) was added to the mixture and the layers were separated. The aqueous layer was extracted with ether (3×50 mL), the organic layer was washed with 10% NaOH solution (3×50 mL), water, and dried over magnesium sulfate. The solvent was concentrated in vacuo to yield a residue and purified by MPLC column chromatography (ethyl acetate/hexane, 3:7) to afford 5.63 g (65%) of 5-ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)phenoxy]propyl]furan (Formula II; R3 =5-ethyl, R4 =hydrogen, R1,R2 =3,5-dimethyl, R5 =2-methyltetrazol-5-yl, Y=1,3-propylene).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05665763
출처 데이터셋uspto-grants-1997_09
ORD IDord-5ab83aaac33e45579e689f23c6f4b675
출처 메모uspto-grants-1997_09