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HRID 865696作成日:2026年10月27日

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

https://huagongshe.com/reaction/865696

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Win 58768HCID 148372—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物5-Ethyl-2-(3-hydroxypropyl)furanHCID 22915401—
溶媒WaterHCID 962—
生成物5-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furanHCID 1595464365.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05567717
出典データセットuspto-grants-1996_10
ORD IDord-5d747741ff1f4beda690ecf2fbb749f3
出典メモuspto-grants-1996_10