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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659174Generated: November 1, 2026

Hydrochloric Acid → HCID 21481314, compound

https://huagongshe.com/reaction/1659174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Ethylpropanedioyl dichlorideHCID 10920924—
ReactantMethyl (2,3-dimethylphenoxy)acetateHCID 13381508—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 21481314HCID 21481314—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of methyl (2,3-dimethylphenoxy)acetate (3.0 g., 0.0155 mole) and 2-ethylmalonyl chloride (2.7 g., 0.016 mole) in methylene chloride (200 ml.) is cooled to 0°C. then treated with aluminum chloride (6.6 g., 0.05 mole) in several portions during a 15 minute period. The reaction is stirred for 2 hours at 0°C., 18 hours at 25°C. then at reflux for 6 hours, cooled and poured into cold 1 N-hydrochloric acid (500 ml.), the organic layer is washed with water, saturated aqueous sodium chloride, dried over magnesium sulfate, then the solvent evaporated at reduced pressure. The crude methyl ester is hydrolyzed by treatment with potassium hydroxide (0.34 g., 0.005 mole) and methanol (20 ml.) at reflux for 1/2 hour, cooled and acidified with aqueous hydrochloric acid affording (1,3-dioxo-2-ethyl-4,5-dimethyl-6-indanyloxy)acetic acid which melts at 187°-193°C. after recrystallization from acid-water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03966966
Source datasetuspto-grants-1976_06
ORD IDord-44734214379c4c369165321957fc05af
Source noteuspto-grants-1976_06