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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2040851Erstellt: 27. Oktober 2026

Ethyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylate → Ethyl 3-hydroxy-3-(2-phenylethynyl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/2040851

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 10082452—
EduktHCID 178419644HCID 178419644—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 3-hydroxy-3-(2-phenylethynyl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 5749381787,2%

Reaktionsschritte

To a solution of ethyl 2-oxo-4-oxa-8-azaspiro[4.5]decane-8-carboxylate (Edwin S. C. Wu, Ronald C. Griffith, James T. Loch III, Alex Kover, Robert J. Murray, George B. Mullen, James C. Blosser, Anthony C. Machulskis, Sally A. McCreedy, J. Med. Chem., 1995, 38 (9), pp 1558-1570, 82 mg, 0.362 mmol) in THF (4 mL) was added dropwise a 1M solution of phenylethynylmagnesium bromide in THF (0.724 mL, 0.724 mmol), stirring at r.t. under anhydrous nitrogen atmosphere. The reaction mixture was stirred at r.t. for 4 h, then at 60° C. for 6 h, then it was quenched with a saturated aqueous solution of ammonium chloride, extracted with EtOAc. The combined organic layers were washed with brine, dried over sodium sulphate and evaporated to dryness in vacuo. The crude was purified by automated flash chromatography (SP1®TM-Biotage; gradient Petroleum Ether-EtOAc from 75:25 to 4:6) affording the title product as yellow solid. Yield: 87.2%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08580962B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-6ac54eb5fe97458d915fec7bffe53092
Quellennotizuspto-grants-2013_11