HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741664Generated: October 31, 2026
Gramine → 3,3-Dicarboxy-4-(indol-3-yl)butanoic acid
https://huagongshe.com/reaction/1741664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gramine | HCID 6890 | — |
| Reactant | Triethyl ethane-1,1,2-tricarboxylate | HCID 81961 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,3-Dicarboxy-4-(indol-3-yl)butanoic acid | HCID 10424353 | — |
Reaction Steps
Gramine (17.4 g) and triethyl 1,1,2-ethanetricarboxylate (24.6 g) were suspended in dry toluene. Sodium (0.05 g) was added and the stirred reaction was heated at reflux for six hours. The reaction mixture was cooled, washed with 2N hydrochloric acid (100 ml) and the organic layer was dried (MgSO4) and evaporated. The resulting brown oil was dissolved in ethanol (400 ml) and potassium hydroxide (56 g) was added. The reaction was heated to reflux for six hours, cooled, poured onto ice and acidified to pH1 with 5N hydrochloric acid. The mixture was saturated with sodium sulphate and extracted with ethyl acetate, dried (Na2SO4), filtered and evaporated. The resulting oil was crystallised from 1,2-dichloroethane (400 ml) to yield the title compound, mp 184°-185° C.; found: C, 55.33; H, 4.67; N, 4.32; C14H13NO6. 0.75(H2O) requires C, 55.17; H, 4.80; N, 4.60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334606 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-24e30f2bc58c453782c7b21f656f7fcd |
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| Source note | uspto-grants-1994_08 |
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