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HRID 1766893作成日:2026年10月27日

Dimethylformamide → Allyl 4-[(4-methoxybenzyl)oxy]-4-oxobutyl succinate

https://huagongshe.com/reaction/1766893

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物4-Methyloxybenzyl chlorideHCID 69993—
反応物Allyl 4-chloro-4-oxobutyrateHCID 17862495—
反応物Sodium OxybateHCID 23663870—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物Allyl 4-[(4-methoxybenzyl)oxy]-4-oxobutyl succinateHCID 5888531870%

反応条件

温度100 °C

反応手順

To a suspension of commercially available sodium 4-hydroxybutyrate (756 mg, 6.00 mmol) in N,N-dimethylformamide (10 ml) was added 4-methoxybenzyl chloride (987 mg, 6.30 mmol), and the mixture was heated at 100° C. for 3 hours. The reaction mixture was cooled, and allyl 4-chloro-4-oxobutyrate (1.06 g, 6.02 mmol) obtained from Example 14-(1), triethylamine (920 μl, 6.60 mmol), and 4-(N,N-dimethylamino)pyridine (10 mg) were added thereto at 0° C. The mixture was stirred at room temperature for 18 hours, and the obtained mixture was diluted with ethyl acetate, then the resulting solution was washed successively with water, a saturated aqueous solution of sodium hydrogen carbonate, a saturated aqueous solution of ammonium chloride, and an aqueous solution of sodium chloride. The solution was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to give an oily residue. The residue was subjected to chromatography on a silica gel (50 g) column (eluent; hexane:ethyl acetate=3:1˜2:1) to afford the title compound (1.52 g, 70% yield) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07230023B2
出典データセットuspto-grants-2007_06
ORD IDord-6a6751f01a83454a82f29511a6fe7c60
出典メモuspto-grants-2007_06