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HRID 982465作成日:2026年10月25日

Hydrochloric Acid → 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione

https://huagongshe.com/reaction/982465

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DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-oneHCID 383405—
反応物3-Methylthio4-n-propoxy-5-benzyloxybenzaldehydeHCID 10471022—
触媒3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
生成物1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dioneHCID 10098743—

反応条件

温度60 °C

反応手順

175 g 3-methylthio-4-n-propoxy-5-benzyloxybenzaldehyde, 135 g of 3,4,5-trimethoxyphenylvinylketone, 10 g of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazoliumbromide, 25 mL of triethyl amine dissolved in 150 ml of dimethylformamide was heated at 60° C. overnight, and the reaction mixture was treated with 400 mL of 1.5N HCl and the aqueous layer decanted. The residue was treated again with fresh 400 mL of 1.5N HCl and decanted two more times. The remaining residue was crystallized from 400 mL of methanol and washed thoroughly with methanol, hexane, and methanol and dried to yield the title compound as a tan solid: NMR(200 MHz, CDCl3) δ 1.03(t, CH2CH2CH3), 1.82(m, CH2CH2CH3), 2.50(s, SCH3), 3.43(s, C(O)CH2CH2CO), 3.94(s, 3 OCH3), 4.11(t, OCH2CH2CH3), 5.17(s, OCH2Ar), 7.30-7.52(m, ArH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04996203
出典データセットuspto-grants-1991_02
ORD IDord-6281e817a89f44aa85263744adfdab80
出典メモuspto-grants-1991_02