HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1391781Erstellt: 26. Oktober 2026
Tetrahydrofuran → Ethyl 3-(4-Hydroxy-3,5-Dimethoxyphenyl)Acrylate
https://huagongshe.com/reaction/1391781
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Syringaldehyde | HCID 8655 | — |
| Edukt | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Produkt | Ethyl 3-(4-Hydroxy-3,5-Dimethoxyphenyl)Acrylate | HCID 6439771 | — |
Reaktionsschritte
To a stirred solution of triethyl phosphonoacetate (0.60 mL, 3.02 mmol) in THF (5 mL) was added portion-wise NaH (60% dispersion in mineral oil, 360 mg, 9.00 mmol) over 2-3 mins. After effervescence had ceased, 4-hydroxy-3,5-dimethoxybenzaldehyde (547 mg, 3.00 mmol) was added portion-wise, washing in with THF (3 mL). More THF (2×2 mL) was added to the thick slurry and the resulting mixture was then heated to reflux for 21 hours. The mixture was then allowed to cool slowly to ambient temperature and the reaction quenched by the careful addition of saturated aqueous NH4Cl (20 mL). The organic solvent was then removed under vacuum and the resulting aqueous mixture was then extracted with DCM (10 mL, 5 mL and then 2 mL) using hydrophobic frits. The filtrate was then treated with Polymer Supported-TsNHNH2 resin (loading 3.22 mmol/g, 1.62 g, 5.23 mmol (3 eq wrt unreacted aldehyde)) and the mixture stirred for 16 hours to remove any unreacted aldehyde. The resin was then removed by filtration washing with DCM (5 mL, 10 mL and then 5 mL) and the filtrate reduced under vacuum to give the title compound (221 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07338960B2 |
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| Quelldatensatz | uspto-grants-2008_03 |
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| ORD ID | ord-98ffb6f561f64b1982844057862db2a3 |
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| Quellennotiz | uspto-grants-2008_03 |
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