HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2085055Erstellt: 26. Oktober 2026
Ethyl Acetate → Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate
https://huagongshe.com/reaction/2085055
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 2-(3-Methoxyphenyl)-1-phenylethan-1-one | HCID 2759614 | — |
| Edukt | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate | HCID 22602685 | 86% |
Reaktionsschritte
Lithium hexamethyidisilazane (88.5 mL, 88.5 mmol) was added to THF (150 mL) at −78° C. After 15 minutes, ethyl acetate (7.79 g, 88.5 mmol) was added over 10 minutes and stirred at −78° C. for 30 minutes. The m-methoxybenzyl phenyl ketone in (10.0 g, 44.25 mmol) THF (100 mL) was added over 15 minutes and kept at that temperature for 3 hours. The reaction mixture was quenched at that temperature with saturated ammonium chloride (15 mL). The reaction mixture was diluted with ether (200 mL) and the organic layer was washed with brine, (100 mL), dried and concentrated to afford the desired product (12 g, 86% yield). NMR was consistent with the desired structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06720315B2 |
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| Quelldatensatz | uspto-grants-2004_04 |
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| ORD ID | ord-0d7cb346805c40b583610cf6d62715e4 |
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| Quellennotiz | uspto-grants-2004_04 |
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