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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1692274Erstellt: 25. Oktober 2026

Tetramethylammonium fluoride → Tert-butyl 3-(5-chloro-2-hydroxyphenyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/1692274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetramethylammonium fluorideHCID 67803—
Edukttert-Butyl3-(2-{[tert-butyl(dimethyl)silyl]oxy)-5-chlorophenyl)azetidine-1-carboxylateHCID 59436503—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 3-(5-chloro-2-hydroxyphenyl)azetidine-1-carboxylateHCID 5943660838%

Reaktionsschritte

To a solution of tert-Butyl 3-(2-{[tert-butyl(dimethyl)silyl]oxy}-5-chlorophenyl)azetidine-1-carboxylate (Preparation 238, 3.1 g, 7.79 mmol) in tetrahydrofuran (80 ml) was added tetramethylammonium fluoride (1.0 g, 10.74 mmol). The mixture was stirred at room temperature for 18 hours before concentrating in vacuo. The residue was partitioned between tert-butyl methyl ether (100 ml) and aqueous sodium hydroxide solution. The organics were dried over sodium sulfate, filtered and evaporated in vacuo to give a reddish brown oil, 2.33 g. This was purified by column chromatography (100 g of silica) eluting with heptane:ethyl acetate (6:4, by volume) to afford the title compound as a reddish brown gum, 850 mg, 38% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153814B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-06238cd149fa435eb08dc2e15e1aa44e
Quellennotizuspto-grants-2012_04