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HRID 82364作成日:2026年10月25日

Hydrochloric Acid → Methyl 2-(4-chlorophenyl)-3-hydroxypropanoate

https://huagongshe.com/reaction/82364

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FormaldehydeHCID 712—
反応物Methyl 4-chlorophenylacetateHCID 104196—
触媒Sodium MethoxideHCID 10942334—
溶媒Dimethyl SulfoxideHCID 679—
生成物Methyl 2-(4-chlorophenyl)-3-hydroxypropanoateHCID 1991473392.2%

反応手順

Methyl 2-(4-chlorophenyl)acetate (36.7 g, 199 mmol) and paraformaldehyde (6.27 g, 209 mmol) were dissolved/suspended in DMSO (400 mL) and treated with NaOMe (537 mg, 9.94 mmol). The mixture was allowed to stir at room temperature for 2 hours to completion by TLC analysis of the crude. The reaction was poured into ice-cold water (700 mL; white emulsion) and neutralized with the addition of 1M HCl solution. The aqueous portion was extracted with ethyl acetate (3×), and the organics were combined. The organic portion was washed with water twice, once with brine, separated, dried over MgSO4, filtered, and concentrated in vacuo to afford the crude product as a yellow oil. The residue was loaded onto a large fitted filtered with silica gel and eluted with 9:1 hexanes:ethyl acetate until the starting material/olefin were collected. The plug was then eluted with 1:1 hexanes:ethyl acetate until the pure desired product was eluted completely. The concentrated pure fractions yielded methyl 2-(4-chlorophenyl)-3-hydroxypropanoate as a colorless oil (39.4 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846681B2
出典データセットuspto-grants-2014_09
ORD IDord-3b794dbd2fff401d8ced19f2ec0b62d5
出典メモuspto-grants-2014_09