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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1013424Erstellt: 26. Oktober 2026

18-Crown-6 → 3-Benzo[b]thiophen-2-yl-acrylic acid tert-butyl ester

https://huagongshe.com/reaction/1013424

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt18-Crown-6HCID 28557—
Edukt1-Benzothiophene-2-carbaldehydeHCID 736500—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
EduktTert-butyl (diphenoxyphosphoryl)acetateHCID 10689048—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Benzo[b]thiophen-2-yl-acrylic acid tert-butyl esterHCID 6720586774,3%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Potassium bis(trimethylsilyl)amide (5.4 g, 0.027 mol) was added to a solution of 18-Crown-6 (13.7 g, 0.052 mol) and (diphenoxy-phosphoryl)-acetic acid tert-butyl ester (9.4 g, 0.027 mol) in dry THF (120 mL) at −78° C. After 30 minutes of stirring at this temperature, benzo[b]thiophene-2-carbaldehyde (4.0 g, 0.024 mol) was added and the reaction was stirred for 3 hours at −78° C. after which the reaction was quenched with saturated ammonium chloride (200 mL). The reaction mix was allowed to come to room temperature and was extracted with ethyl acetate (3×200 mL) and the combined organic extracts were washed with 10% HCl (200 mL), brine (200 mL), and dried over MgSO4. The solvent was evaporated in vacuo leaving the crude product that was purified by column chromatography (SiO2) using a 5-40% ethylacetate-hexane gradient to afford the subtitle compound (4.64 g, yield: 74%). MS calculated for C15H16O2S +H: 261, observed: 261.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07981919B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-50fe8b81151c4653a48db4325c88f59e
Quellennotizuspto-grants-2011_07