HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278479Erstellt: 25. Oktober 2026
Triethylamine → Methyl 3-(4-hydroxy-3-oxobutyl)phenylacetate
https://huagongshe.com/reaction/278479
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Butene-1,2-diol | HCID 10338 | — |
| Edukt | Tributylphosphine | HCID 13831 | — |
| Edukt | Methyl 2-(3-bromophenyl)acetate | HCID 11746402 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl 3-(4-hydroxy-3-oxobutyl)phenylacetate | HCID 22628477 | 24,4% |
Reaktionsschritte
To a stirred solution of Pd (OAc)2 (75 mg, 0.34 mmol), nBu3P (136 mg, 0.67 mmol), and Et3N (442 mg, 4.37 mmol) in DMF (10 ml) was added 3-butene-1,2-diol (296 mg, 3.36 mmol) followed by methyl 3-bromophenylacetate (1.0 g, 4.37 mmol), and the reaction mixture was stirred at 100° C. for 5 h. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (magnesium sulfate) and evaporated in vacuo. The residue was purified by silica gel (25 g) column chromatography eluting with toluene/ethyl acetate (20:1) to give methyl 3-(4-hydroxy-3-oxobutyl)phenylacetate (193 mg, 24.4%) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06359145B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-083726f3412d4d3c8c9aca3e9842e928 |
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| Quellennotiz | uspto-grants-2002_03 |
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