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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1766893생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1766893

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물4-Methyloxybenzyl chlorideHCID 69993—
반응물Allyl 4-chloro-4-oxobutyrateHCID 17862495—
반응물Sodium OxybateHCID 23663870—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물Allyl 4-[(4-methoxybenzyl)oxy]-4-oxobutyl succinateHCID 5888531870%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07230023B2
출처 데이터셋uspto-grants-2007_06
ORD IDord-6a6751f01a83454a82f29511a6fe7c60
출처 메모uspto-grants-2007_06