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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1170403Erstellt: 27. Oktober 2026

2-Methyl-2-butene → (S)-4-acetoxypent-2-ynoic acid

https://huagongshe.com/reaction/1170403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-2-buteneHCID 10553—
Edukt(S)-4-formylbut-3-yn-2-yl acetateHCID 11499231—
EduktSodium ChloriteHCID 23668197—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
Produkt(S)-4-acetoxypent-2-ynoic acidHCID 59552181100,6%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07825267B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-bb1f06fc8da3419587d91806cc391f34
Quellennotizuspto-grants-2010_11