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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79504Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/79504

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFormaldehydeHCID 712—
EduktMethyl 4-chlorophenylacetateHCID 104196—
KatalysatorSodium MethoxideHCID 10942334—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktMethyl 2-(4-chlorophenyl)-3-hydroxypropanoateHCID 1991473392,2%

Reaktionsschritte

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; emulsion) and neutralized with the addition of 1M HCl solution. The aqueous layer was extracted with ethyl acetate (3×), and the organics were combined. The organic layer was washed with water (2×), brine (1×), separated, dried over MgSO4, filtered, and concentrated in vacuo to afford the crude product as an oil. The residue was loaded onto a large fritted 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 an oil (39.4 g, 92%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841304B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-f355148a131e46a1adb6b871665d0c23
Quellennotizuspto-grants-2014_09