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HRID 257356생성일: 2026년 10월 25일

Potassium Carbonate → Methyl 2-(5-chloro-2-formylphenoxy)propionate

https://huagongshe.com/reaction/257356

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Methyl 2-bromopropionateHCID 95576—
반응물4-Chloro-2-hydroxybenzaldehydeHCID 520101—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(5-chloro-2-formylphenoxy)propionateHCID 5380006018.2%

반응 조건

온도80 °C

반응 단계

A mixture of 22.0 g (0.141 mole) of 4-chlorosalicylaldehyde, 30 g (0.22 mole) of anhydrous potassium carbonate, and 30.0 g (0.184 mole) of methyl 2-bromopropionate in 120 mL of N,N-dimethylformamide was heated at 80° C. for approximately 17 hours. At the end of that period, the reaction mixture was poured over ice and extracted successively with diethyl ether and ethyl acetate. The combined extracts were washed with water, dried over anhydrous magnesium sulfate, and filtered. The solvents were then evaporated under reduced pressure, leaving a residue weighing 20 g. This residue was purified by placing it on a silica gel column and eluting with diethyl ether/petroleum ether (25/75). After the product-containing fractions were combined and the solvents evaporated under reduced pressure, 6.23 g of methyl 2-(5-chloro-2-formylphenoxy)propionate was isolated as a yellow liquid. Similarly, other fractions were combined and evaporated, yielding 1.69 g of methyl 2-(3-chloro-2-formylphenoxy)propionate as a yellow liquid. The NMR spectra of both compounds were consistent with proposed structure of each. This reaction was repeated several times.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262390
출처 데이터셋uspto-grants-1993_11
ORD IDord-efb1b7ad488b4c87892270c806498fbd
출처 메모uspto-grants-1993_11