HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902525Generated: October 30, 2026
Hydrochloric Acid → 3-Carboxy-1,4-dimethyl-1H-pyrrole-2-acetic acid
https://huagongshe.com/reaction/1902525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Acetonedicarboxylic acid | HCID 68328 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Carboxy-1,4-dimethyl-1H-pyrrole-2-acetic acid | HCID 118465 | 85% |
Reaction Steps
To 1200 parts of cold water (about 5° C.) there are added 292 parts of 3-oxo-pentanedioic acid and the reaction mixture is further cooled to -5° C. 1770 Parts of methanamine 35% in water are then added slowly while stirring and cooling to a temperature between -5° C. and 5° C. The reaction mixture is further cooled to about -15° C. Then 370 parts of 1-chloro-2-propanone are added portionwise under vigorous cooling. An exothermic reaction takes place and the temperature of the mixture raises to about 15° C. It is again cooled to about 0° C. and further stirred at this temperature for about 16 hours. The reaction mixture is then poured onto a mixture of 4000 parts of ice and 2200 parts of concentrated hydrochloric acid solution (10.5 N) and stirring is continued for 20 minutes. The product is filtered off and dried in vacuo at 50° C. over CaCl2, yielding 335 parts (85%) of 3-carboxy-1,4-dimethyl-1H-pyrrole-2-acetic acid, mp. 192.8°-194.6° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04363918 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-fd971e48a7cf45f9a036b5c8ead44c01 |
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| Source note | uspto-grants-1982_12 |
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