Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methyl-2-butene | HCID 10553 | — |
| Edukt | (S)-4-formylbut-3-yn-2-yl acetate | HCID 11499231 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | (S)-4-acetoxypent-2-ynoic acid | HCID 59552181 | 100,6% |
Reaktionsschritte
To a solution of 9 (133 mg, 0.949 mmol) and 2-methyl-2-butene (1.20 mL, 14.2 mmol) in tBuOH (1.9 mL) was added the mixture of NaClO2 (257 mg, 2.84 mmol) and NaH2PO4 (393 mg, 2.84 mmol) in H2O (1.9 mL) at 23° C. The resulting mixture was stirred for 20 min at the same temperature and quenched by 1 N aqueous HCl (3 mL) at 0° C. The mixture was poured into a separatory funnel and diluted with EtOAc (3 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3×4 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. Purification of the residue via flash chromatography (silica gel 15 mL; 50→100% EtOAc in hexanes containing 1.0% acetic acid) afforded acid 10 (149 mg, quantitative yield) as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08309599B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-388c0eb8c23f4f9eacdd01bceaa2f18c |
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| Quellennotiz | uspto-grants-2012_11 |
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