戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 377816作成日:2026年10月27日

Hydrochloric Acid → 1-(4'-Methylphenyl)-4,4-diethoxybutan-1,3-dione

https://huagongshe.com/reaction/377816

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p-METHYLACETOPHENONEHCID 8500—
反応物Ethyl diethoxyacetateHCID 80169—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4'-Methylphenyl)-4,4-diethoxybutan-1,3-dioneHCID 15461751—

反応条件

温度-70 °C

反応手順

A 1.0 M solution of lithium hexamethyldisilazide in THF (310 mmol, 310 mL) was diluted with 20 mL of THF and cooled to -70° C. (internal temperature) with an acetone/dry ice bath under N2. A solution of 4'-methylacetophenone (150 mmol, 20.1 g, 20 mL) in 50 mL of tetrahydrofuran (THF) was added dropwise over a 15 min period, keeping the internal temperature below -60° C. After 1 h, the cooling bath was removed and the temperature was allowed to rise to -25° C. The reaction flask was immersed in an ice/acetone bath and a solution of ethyl diethoxyacetate (160 mmol, 28 g, 28.6 mL) in 20 mL of THF was added dropwise; during the addition, the internal temperature was kept below 0° C. The brown-red solution was stirred for 24 h and was re-cooled to 0° C. Aqueous HCl (3N, 618 mmol, 206 mL) was added carefully (temperature kept below 20° C.) to bring the pH to 3-4. The layers were separated and the aqueous layer was extracted with 200 mL of ether. The combined organic layers were washed twice with brine, dried over Na2SO4, and concentrated to give 40.3 g (100%) Cpd. 46 as an orange oil; 1H NMR (CDCl3, 300 MHz) 1.30 (t, 6H, J=7), 2.42 (s, 3H), 3.5-3.8 (complex, 4H), 4.90 (s, 1H), 6.58 (s, 1H), 7.28 (d, 2H, J=8), 7.74 (d, 2H, J=8), 15.8 (broad s, 1H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06028202
出典データセットuspto-grants-2000_02
ORD IDord-91f3c7e406294f45ab0306756a8d517e
出典メモuspto-grants-2000_02