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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781787Generated: October 27, 2026

Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester → 3-(2-Chlorophenyl)propanoic acid

https://huagongshe.com/reaction/1781787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
ReactantDiethyl 2-(2-chlorobenzyl)malonateHCID 12661049—
SolventHydrochloric AcidHCID 313—
Product3-(2-Chlorophenyl)propanoic acidHCID 9567693.4%

Reaction Steps

To a 50 liter flask was added diethyl o-chlorobenzylmalonate (6067 g, 21.31 mol), glacial acetic. acid (1090 mL), and concentrated hydrochloric acid (16,000 mL). The reaction was then heated at reflux for 21 hours and 13 minutes. Additional concentrated hydrochloric acid (1840 mL, 5520 mL total) was added at 3.5, 13.5, and 17 hours into the reflux. The reaction was cooled to 0°±2° C. and the resulting solid was collected by suction filtration and washed with water (4 L). The solid was suspended in water (8 L) and the slurry was stirred for five minutes. The solid was collected by suction filtration and washed with water (20 L). The filtrate was pH 2 and tested positive for chlorine. The solid was then washed seven times in the following manner; the solid was suspended in water (8 L) and stirred for approximately ten minutes. The solid was collected by suction filtration and washed with water (4 L). The filtrate was tested for chloride ion and the pH was recorded. The final filtrate was pH 4.5-5 and tested negative to the presence of chloride ion. A total of 100 liters of water was used to wash the solid. The solid was dried under vacuum at 35°±3° C. for 70 hours to give crude β-2-chlorophenylpropionic acid (3653 g, 93.4%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633404
Source datasetuspto-grants-1997_05
ORD IDord-1b27e7ea017449b68acfe3c2babcd2ac
Source noteuspto-grants-1997_05