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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598883Generated: November 1, 2026

Methyl chloroacetate → HCID 53919154, compound

https://huagongshe.com/reaction/1598883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroacetateHCID 7295—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-acetylsalicylateHCID 85444—
SolventDimethylformamideHCID 6228—
ProductHCID 53919154HCID 53919154—

Reaction Steps

To 1.16 g of 5-acetylsalicylic acid, methyl ester in 10 mL of N,N-dimethylformamide is added 1 g of chloroacetic acid, methyl ester and 1.2 g of potassium carbonate. After stirring this mixture at ambient temperature for 16 hours the reaction is filtered, diluted with ethyl acetate, and washed once with water and twice with brine. The ethyl acetate is dried with magnesium sulfate, filtered, and evaporated to give 5-acetyl-2-(carboxymethoxy)benzoic acid as a crude product. Crystallization from methanol at -15° C. gives 0.6 g of white crystals. 1H-NMR (CDCl3): 8.5 ppm (1H, d), 8.1 ppm (1H, dd), 6.9 ppm (1H, d), 4.8 ppm (2H, s), 4.0 ppm (3H, s), 3.8 ppm (3H, s), 2.6 ppm (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739116
Source datasetuspto-grants-1998_04
ORD IDord-6a0983430f454f2c85faccb92a18fdc2
Source noteuspto-grants-1998_04