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HRID 1589362作成日:2026年10月25日

Hydrochloric Acid → 1-(3,4-Dimethoxyphenyl)-7-(4-methoxyphenyl)-2-nitro-5-heptanone

https://huagongshe.com/reaction/1589362

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzene, 1,2-dimethoxy-4-(2-nitroethyl)-HCID 10036050—
反応物1-Iodo-5-(4-methoxyphenyl)-3-pentanoneHCID 13065019—
反応物Nitro ketoneHCID 54223030—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3,4-Dimethoxyphenyl)-7-(4-methoxyphenyl)-2-nitro-5-heptanoneHCID 13065020—

反応手順

To a solution of 15 g. (0.071 mole) of 2-(3,4-dimethoxyphenyl)-1-nitroethane in 200 ml. of dry tetrahydrofuran was added 33.45 g. (0.08 mole) of 40% Triton B at room temperature. The solution was stirred at room temperature for 14 minutes under N2. 22.6 g. (0.071 mole) of 1-iodo-5-(4-methoxyphenyl)-3-pentanone was then added in portions. The mixture was heated at 50°-55° for 2 hours under N2 until no more starting material was detected on TLC, and then cooled to room temperature. The resulting reaction solution was poured into cold dil. HCl and extracted with ethyl acetate. The organic layer was dried over anhydrous MgSO4. The crude material was chromatographed on Florisil to provide 22 g. of desired nitro ketone derivative. Recrystallization from 80% ethanol gave a white solid which has m.p. 87°-89° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04569941
出典データセットuspto-grants-1986_02
ORD IDord-4e876742b4d74499b495eda206c5d6e7
出典メモuspto-grants-1986_02