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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675842Generated: November 1, 2026

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

https://huagongshe.com/reaction/1675842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantMethyl 4-chlorophenylacetateHCID 104196—
CatalystSodium MethoxideHCID 10942334—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 2-(4-chlorophenyl)-3-hydroxypropanoateHCID 1991473392.2%

Reaction Steps

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 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 a colorless oil (39.4 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003651B2
Source datasetuspto-grants-2011_08
ORD IDord-8736170583de429b9e3c33e9527d7721
Source noteuspto-grants-2011_08