HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60037Erstellt: 23. Oktober 2026
Benzyl Bromide → Methyl 2-(2-methoxyphenyl)-3-phenylpropanoate
https://huagongshe.com/de/reaction/60037
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Methyl 2-methoxybenzeneacetate | HCID 99590 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Lösungsmittel | Tetrahydrofuran heptane | HCID 21263495 | — |
| Produkt | Methyl 2-(2-methoxyphenyl)-3-phenylpropanoate | HCID 66695010 | 35% |
Reaktionsschritte
A 500 mL round-bottom flask is charged with methyl 2-(2-methoxyphenyl)acetate (8.496 g, 47 mmol, 1 eq) and THF (200 mL). The homogeneous mixture is cooled to 0° C. in an ice bath. Lithium diisopropyl amide (23.5 mL of a 2.0M solution in heptane/THF) is added, maintaining a temperature less than 3° C. The reaction is stirred 45 minutes at this reduced temperature. Benzyl bromide (5.6 mL, 47 mmol, 1 eq) is added dropwise. The reaction is allowed to gradually warm to room temperature and is stirred for 18 hours. The reaction is quenched with 1N HCl and extracted 3 times with equal portions of EtOAc. The combined extracts are washed with H2O and brine, dried over Na2SO4, filtered, and concentrated. The residue is purified over silica to afford 4.433 g (35%) of the desired compound. ESI+ MS 293 (M+Na).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09440963B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-b727acaf84d04100872220a5c37a1ffb |
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| Quellennotiz | uspto-grants-2016_09 |
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