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HRID 979376作成日:2026年10月25日

Potassium Fluoride → 1-(3,4-Dimethoxyphenyl)-2-nitro-6-cyano-6-(prop-2-yl)-6-(3,4-dimethoxyphenyl)hexan-3-ol

https://huagongshe.com/reaction/979376

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium FluorideHCID 522689—
反応物3-(3,4-Dimethoxyphenyl)-2-methyl-6-oxohexane-3-carbonitrileHCID 3015370—
反応物Benzene, 1,2-dimethoxy-4-(2-nitroethyl)-HCID 10036050—
溶媒IsopropanolHCID 3776—
生成物1-(3,4-Dimethoxyphenyl)-2-nitro-6-cyano-6-(prop-2-yl)-6-(3,4-dimethoxyphenyl)hexan-3-olHCID 1374575473.9%

反応手順

A mixture of 2-(3,4-dimethoxyphenyl)-1-nitroethane (4, 135 g, 0.64 mol), 2-(3,4-dimethoxyphenyl)-2-(3-oxopropyl)-2-isopropylacetonitrile (7, 156 g, 0.57 mol) and KF (19.3 g, anhydrous, Aldrich) in 2-propanol (2.0 L) was heated to 50°-55° C. for about 40 hours. The mixture was then cooled to room temperature and the isopropanol removed in vacuo. The residue was dissolved in CH2Cl2 (1.6 L) and filtered through Celite (50 g). The filtrate was extracted with saturated aqueous NaHCO3 (2×500 mL), the organic layer evaporated, and the product recrystallized from ethyl acetate-hexane (1:1) to yield 1-(3,4-dimethoxyphenyl)-2-nitro-6-cyano-6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexan-3-ol (8, 205 g, m.p. 171°-173° C., MS m/e 486 (M+)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04667038
出典データセットuspto-grants-1987_05
ORD IDord-a4b5f385c0054b7390e1b66ef8677de2
出典メモuspto-grants-1987_05