HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 523248Erstellt: 26. Oktober 2026
Acetic Acid → 5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid
https://huagongshe.com/reaction/523248
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Ethyl 3-oxocyclohexanecarboxylate | HCID 118096 | — |
| Edukt | 4-Bromo-2-hydrazinyl-5-methylbenzoic acid hydrochloride | HCID 117761019 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid | HCID 117775453 | 55% |
Reaktionsschritte
A mixture of 4-bromo-2-hydrazinyl-5-methylbenzoic acid hydrochloride (2.17 g, 7.71 mmol), ethyl 3-oxocyclohexanecarboxylate (1.44 g, 8.48 mmol) and acetic acid (1.32 mL, 23.1 mmol) in toluene (40 mL) was heated in an oil bath at 117° C. for 5 h. The mixture was concentrated and dried under vacuum, and the residue was diluted with toluene (18 mL) and TFA (4.5 mL). The mixture was heated at 90° C. overnight. The cooled mixture was diluted with EtOAc, sonicated, and the precipitate was collected by filtration and washed with EtOAc to give a yellow solid. The filtrate was concentrated and the residue was suspended in EtOAc with sonication. The precipitate was collected by filtration and combined with the first precipitate. The solid was triturated with MeOH to give 5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid as a pale yellow solid (1.60 g, 55% yield). Mass spectrum m/z 380, 382 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09334290B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-3757c9ebbabb4d82bc41aa9394744026 |
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| Quellennotiz | uspto-grants-2016_05 |
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