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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419615Generated: November 1, 2026

1,1-Cyclopropanedicarboxylic acid, 1,1-dimethyl ester → 1,1-Cyclopropanedicarboxylic acid

https://huagongshe.com/reaction/1419615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Cyclopropanedicarboxylic acid, 1,1-dimethyl esterHCID 2769539—
SolventWaterHCID 962—
Product1,1-Cyclopropanedicarboxylic acidHCID 69017—

Reaction Steps

The glass pipe of the above-described apparatus is charged with 600 ml of the ion exchanger LEWATIT® SP 112 (in the H+ form) and closed on both sides by sintered glass disks. The glass flask contains 500 g of dimethyl cyclopropane-1,1-dicarboxylate (MOD, 98.8%, 3.12 mol) and 750 ml of demineralized water. At a reduced pressure of 700 mbar the contents is heated to boiling (89°-92° C.), the liquids being recirculated by pumping from the flask via the ion exchanger column. At a reflux ratio of from 8:1-15:1 methanol distills off at from 56°-58° C. After 9-10 hours the saponification is complete. After cooling, the apparatus is flushed with water. The combined aqueous solutions are then extracted with 750 ml and twice with 250 ml of methyl t-butyl ether. The ether removed by largely distillation and replaced by 850 ml of toluene. The ether is then removed by distillation completely, and CDA crystallizes in the process. The crystals are removed by filtration, washed with toluene and dried. The final weight and the analytical data are shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886219
Source datasetuspto-grants-1999_03
ORD IDord-5150de380a854ee6a376cb5580f1b175
Source noteuspto-grants-1999_03