HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405340Generated: October 29, 2026
Potassium Carbonate → [(4-chloro-2-formyl-6-methylphenyl)oxy]acetic Acid
https://huagongshe.com/reaction/2405340
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 5-Chloro-2-hydroxy-3-methylbenzaldehyde | HCID 2774358 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [(4-chloro-2-formyl-6-methylphenyl)oxy]acetic Acid | HCID 86674828 | 80% |
Reaction Steps
A solution of 5-chloro-2-hydroxy-3-methylbenzaldehyde (5.86 mmol) in acetonitrile (30 mL) was treated with potassium carbonate (17.59 mmol). The reaction mixture was stirred for 30 min and was then treated with methyl bromoacetate (7.03 mmol). The resulting mixture was stirred at room temperature overnight. Analysis by LCMS indicated the formation of the desired intermediate ester, and the reaction mixture was concentrated to dryness in vacuo. The crude material was dissolved in a 3:1 methanol:water mixture (20 mL) and was heated to 50° C. with stirring. The reaction was then cooled to room temperature and was acidified to pH˜3 using 1N aq HCl. The methanol was removed in vacuo and the resulting aqueous suspension was diluted with water (100 mL) and was extracted with dichloromethane. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting beige solid was used without further purification (1.07 grams, 80% yield). MS(ES)+ m/e 229.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802864B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-0f0ce19c27e6490886cad1d2bb403110 |
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| Source note | uspto-grants-2014_08 |
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