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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Cyclopropanedicarboxylic acid, 1,1-dimethyl ester | HCID 2769539 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,1-Cyclopropanedicarboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886219 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-5150de380a854ee6a376cb5580f1b175 |
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| Source note | uspto-grants-1999_03 |
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