HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19405Erstellt: 23. Oktober 2026
Ethyl 2-(diphenylmethyleneamino)acetate → (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester
https://huagongshe.com/de/reaction/19405
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl 2-(diphenylmethyleneamino)acetate | HCID 319508 | — |
| Edukt | (S)-(+)-1-Iodo-2-methylbutane | HCID 5702528 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester | HCID 86635244 | 74% |
Reaktionsschritte
A solution of (benzhydrylidene-amino)-acetic acid ethyl ester (5.48 g, 20.5 mmol) in tetrahydrofuran (40 mL) was treated with potassium t-butoxide (2.83 g, 25.26 mmol) and stirred at 0° C. for 35 min. At this time a solution of (S)-1-iodo-2-methyl-butane (5.00 g, 25.25 mmol) in tetrahydrofuran (20 mL) was added via syringe and the resulting solution stirred at 0° C. for 10 min and then room temperature overnight. The reaction mixture was concentrated in vacuo and the residue partitioned between diethyl ether and dilute aqueous hydrochloric acid. The layers were separated, and the organic layer was washed with brine and concentrated in vacuo. The residue was purified by ISCO flash chromatography (RediSep silica 120 g, 0% to 10% ethyl acetate/hexanes) which afforded (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester (5.09 g, 74%) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741327B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-e2b1e4a3f0e64d58bf4a398c4d0d1a9d |
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| Quellennotiz | uspto-grants-2010_06 |
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