HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18362Erstellt: 24. Oktober 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (S)-1-Phenylethyl 2-(2-fluorophenyl)acetate
https://huagongshe.com/de/reaction/18362
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | Benzeneacetic acid, 2-fluoro- | HCID 67979 | — |
| Edukt | 1-Phenylethanol, (S)- | HCID 443135 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (S)-1-Phenylethyl 2-(2-fluorophenyl)acetate | HCID 66648658 | 92% |
Reaktionsschritte
A mixture of 2-fluorophenylacetic acid (5.45 g, 35.4 mmol), (S)-1-phenylethanol (5.62 g, 46.0 mmol), EDCI (8.82 g, 46.0 mmol) and DMAP (0.561 g, 4.60 mmol) in CH2Cl2 (100 mL) was stirred at room temperature for 12 hours. The solvent was then concentrated and the residue partitioned with H2O-ethyl acetate. The phases were separated and the aqueous layer back-extracted with ethyl acetate (2×). The combined organic phases were washed (H2O, brine), dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (Biotage/0-20% ethyl acetate-hexane) to provide the title compound as a colorless oil (8.38 g, 92%). 1H NMR (400 MHz, CD3OD) δ 7.32-7.23 (m, 7H), 7.10-7.04 (m, 2), 5.85 (q, J=6.5 Hz, 1H), 3.71 (s, 2H), 1.48 (d, J=6.5 Hz, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741347B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-6b40bd51172d45dcb4835c47947189e3 |
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| Quellennotiz | uspto-grants-2010_06 |
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