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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1896010Erstellt: 25. Oktober 2026

Boron trifluoride etherate → tert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1896010

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
EduktLithium phenylacetylideHCID 3437284—
Edukttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylateHCID 8662734691,9%

Reaktionsbedingungen

Temperatur-75 °C

Reaktionsschritte

Boron trifluoride diethyl etherate (0.131 mL, 1.03 mmol) followed by lithium phenylacetylide (1M in THF, 1.03 mL, 1.03 mmol) was dropped into a solution of Compound 256a (200 mg, 0.938 mmol) in THF (5 mL) stirred at −75° C. under nitrogen atmosphere. Stirring and cooling were kept on for 2 h and after overnight stirring at r.t., the reaction mixture was quenched with water and EtOAc. The combined extracts were washed, dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (EtOAc—Petroleum Ether 85:15) affording the title product (272 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08518916B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-aad17222f93344df9a3fc42be36177bf
Quellennotizuspto-grants-2013_08