HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661488Generated: November 4, 2026
Ethyl Acetoacetate → 4-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acid
https://huagongshe.com/reaction/661488
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Amino-5-oxohexanoic acid hydrochloride | HCID 71386672 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Monosodium phosphate | HCID 23672064 | — |
| Product | 4-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acid | HCID 59376020 | 71% |
Reaction Steps
6-amino-5-oxohexanoic acid hydrochloride (S1) 22.44 g (0.12 mol) (Lartillot, Serge. et al, Bulletin de la Societe Chimique de France, 1964, 4:783) was solved in about 6.1 L sodium dihydrogen phosphate buffer (300 g sodium dihydrogen phosphate was solved in 6 L water, then Saturated sodium hydroxide aqueous solution was added until a pH of about 6.5 was reached), and ethyl acetoacetate 16.12 g (0.12 mol) was added to the above-mentioned solution. The reaction solution was refluxed for half an hour, cooled to room temperature and Na2CO3 was added until a pH of about 8 was reached. The mixture was extracted with 100 ml CHCl3 and Aqueous phase was acidified with 6 mol/L HCl to pH 1. The brown solid was collected by filtration, washed with water and dried in vacuum condition to give 20.29 g (71%) 4-(4-(ethoxycarbonyl)-5-methyl-1H-pyrrol-3-yl)butanoic acid (S2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084621B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-ab1722fc6e934c0da08fe8402505c25d |
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| Source note | uspto-grants-2011_12 |
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