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HRID 1085636作成日:2026年10月25日

1-Bromopropane → 1-(3-Iodo-5-methoxy-4-propoxyphenyl)-4-(3,4,5-trimethoxyphenyl)-1,4-butanedione

https://huagongshe.com/reaction/1085636

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromopropaneHCID 7840—
反応物Potassium CarbonateHCID 11430—
反応物1-(5-Iodo-4-hydroxy-3-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl)butan-1,4-dioneHCID 15718033—
溶媒DimethylformamideHCID 6228—
生成物1-(3-Iodo-5-methoxy-4-propoxyphenyl)-4-(3,4,5-trimethoxyphenyl)-1,4-butanedioneHCID 15718028—

反応条件

温度70 °C

反応手順

n-Propyl bromide (29.2 mL, 0.32 mole) was added to a solution of 1-(5-iodo-4-hydroxy-3-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl)butan-1,4-dione (100 g, 0.2 mole) in DMF (400 mL) containing potassium carbonate (96 g, 0.35 mole). The mixture was stirred at 70° C. for 2 hours during which time starting material disappeared. The mixture was cooled, filtered, and extracted with ethyl acetate, and the extract was washed with water and brine, dried over anhydrous MgSO4, and evaporated in vacuo to afford the crude product. Crystallization from ether/hexane gave the title compound as white crystals, m.p. 120°-121° C. NMR (CDCl3) δ 1.08 (t, J=7.5 Hz, CH2CH2CH3) 1.87 (m, CH2CH2CH3), 2.41 (t, J=4 Hz, COCH2CH2CO), 3.90 and 3.94 (s, u Ar OCH3), 4.04 (t, J=8 Hz, OCH2CH2CH3), 7.28 (s, trimethoxyphenyl H-2, H-6), 7.51 (d, J=1.5 Hz, Iodophenyl 'H-6), 8.06 (d, J=1.5 Hz, Iodophenyl 'H-2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05010100
出典データセットuspto-grants-1991_04
ORD IDord-ef0db20f7803405aa080239b2cf970a0
出典メモuspto-grants-1991_04