HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79504Generated: October 25, 2026
Hydrochloric Acid → Methyl 2-(4-chlorophenyl)-3-hydroxypropanoate
https://huagongshe.com/reaction/79504
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methyl 4-chlorophenylacetate | HCID 104196 | — |
| Catalyst | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Methyl 2-(4-chlorophenyl)-3-hydroxypropanoate | HCID 19914733 | 92.2% |
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; 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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841304B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f355148a131e46a1adb6b871665d0c23 |
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| Source note | uspto-grants-2014_09 |
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