Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Methyl-1-butene | HCID 11240 | — |
| Reactant | Sodium Phosphate, Monobasic, Monohydrate | HCID 516949 | — |
| Reactant | Ethyl 5-formyl-4-methyl-1H-pyrrole-2-carboxylate | HCID 9855648 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 68487354 | HCID 68487354 | — |
Reaction Steps
To a solution of ethyl 5-formyl-4-methyl-1H-pyrrole-2-carboxylate (0.40 g, 2.21 mmol) in t-BuOH (25 mL) was added 2-methylbutene as a 2M solution (38 mL, 76.0 mmol). In a separate flask sodium dihydrogen phosphate monohydrate (2.1 g, 15.2 mmol) and sodium chlorite (1.8 g, 19.9 mmol) were dissolved in water (25 mL). The aqueous solution was added to the alcoholic reaction mixture dropwise and stirred for 3 h. Additional sodium dihydrogen phosphate monohydrate (1.05 g, 7.73 mmol) and sodium chlorite (0.9 g, 9.95 mmol) dissolved in water (10 mL) were added and the reaction mixture stirred an additional 2 h. The solution was acidified with aqueous 5% HCl to a pH ˜4 and extracted with EtOAc (3×25 mL). The organic layers combined, dried over sodium sulfate, filtered and the solvent evaporated. Purification by column chromatography twice afforded 4-chloro-5-[(ethyloxy)carbonyl]-3-methyl-1H-pyrrole-2-carboxylic acid (0.10 g, 20%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 12.32 (br. s., 1H) 4.24 (q, 2H) 2.19 (s, 3H) 1.28 (t, 3H). MS: m/z 232.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-773658a162bf4c02bd0d9af39481fb75 |
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| Source note | uspto-grants-2012_11 |
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