HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307915Generated: November 1, 2026
Acetic Acid → methyl 3-(2-methoxy-2-oxoethyl)-1H-indole-2-carboxylate
https://huagongshe.com/reaction/2307915
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Dimethyl alpha-ketoglutarate | HCID 25775 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl 3-(2-methoxy-2-oxoethyl)-1H-indole-2-carboxylate | HCID 10332197 | — |
Reaction Steps
Phenyl hydrazine (5.7 ml), dimethyl 2-oxoglutarate (10 g) and acetic acid (1.0 ml) in methanol (100 ml) were heated at reflux for 1 hour, then concentrated in in vacuo. The crude hydrazone (13 g) was dissolved in saturated methanolic hydrochloric acid (350 ml) and heated to 75° C. for 16 hours with continual stirring. The reaction was diluted with water (200 ml) and extracted with dichloromethane. Combined organic extracts were washed with saturated aqueous sodium hydrogencarbonate solution, water, saturated aqueous sodium chloride solution and dried (MgSO4). The solvent was removed in vacuo to give a yellow crystalline solid (7.0 g); NMR d (CD3SOCD3) 3.59 (s, 3H), 3.83 (s, 3H), 4.12 (s, 2H), 7.06 (t, 1H), 7.26 (t, 1H), 7.41 (d, 1H), 7.63 (d, 1H), 11.76 (brs, 1H); M/z (−) 246 (M−H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06833387B1 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-5f8f7c4c721143ba9b148d60a787bbfe |
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| Source note | uspto-grants-2004_12 |
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