HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15496Erstellt: 25. Oktober 2026
Potassium Carbonate → Indoline-2-carboxylic acid, (S)-
https://huagongshe.com/reaction/15496
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Bromophenylalanine | HCID 193338 | — |
| Katalysator | Cuprous chloride | HCID 62652 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Indoline-2-carboxylic acid, (S)- | HCID 2733920 | 69% |
Reaktionsschritte
A flask was charged successively with 4.89 g (20.0 mmol) (S)-2-bromophenylalanine, 2.93 g (21.2 mmol) K2CO3, 0.2 mg CuCl (2.9 mmol) and 39.7 g H2O. The reactor was flushed with argon and then kept under a slow stream of argon. The reaction mixture was stirred and heated until 95° C. and kept at this temperature. Samples were taken regularly and analyzed by HPLC. After 4 h hour full conversion of (S)-2-bromophenylalanine was found. The reaction mixture was cooled to 25° C. Then the reaction mixture was acidified with 4.47 g 5M aqueous HCl until pH=4.4. The precipitated (S)-2,3-dihydro-1H-indole-2-carboxylic acid was isolated by filtration and washed with 2×10 mL H2O. Found after drying 2.24 g (13.7 mmol) (S)-2,3-dihydro-1H-indole-2-carboxylic acid. Yield 69%, ee>99%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732621B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-4eadd03d57b64ca3904388a9a3414166 |
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| Quellennotiz | uspto-grants-2010_06 |
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