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HRID 1951395作成日:2026年10月25日

Acetic Acid → 4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methylbenzonitrile

https://huagongshe.com/reaction/1951395

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PiperidineHCID 8082—
反応物AcetylacetoneHCID 31261—
反応物4-Formyl-3-methylbenzonitrileHCID 10909695—
溶媒DichloromethaneHCID 6344—
生成物4-(2-Acetyl-3-oxobut-1-en-1-yl)-3-methylbenzonitrileHCID 59603030—

反応手順

950 mg (6.54 mmol) of 3-methyl-4-formylbenzonitrile [S. Levesque et al., Bioorg. Med. Chem. Lett. 11, 3161-3164 (2000], 655.2 mg (6.544 mmol) of 2,4-pentanedione, 589.5 mg (9.82 mmol) of acetic acid and 111.5 mg (1.31 mmol) of piperidine are dissolved in 35 ml of dichloromethane and heated under reflux with an inverse water trap overnight. Cooling is followed by washing twice with water, and the organic phase is dried with magnesium sulfate. The solvent is removed in a rotary evaporator and the residue is purified by column chromatography (silica gel, mobile phase: initially dichloromethane, then isohexane/ethyl acetate 3:1). After concentration of the product fractions, the residue is crystallized from diethyl ether and dried under high vacuum. 1.12 g (75.3% of theory) of the title compound are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08404709B2
出典データセットuspto-grants-2013_03
ORD IDord-ffc25bb006974dd58b30decbfe449b09
出典メモuspto-grants-2013_03