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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 465612Erstellt: 24. Oktober 2026

Bromoacetonitrile → 7-Cyano-5-oxoheptanoic acid

https://huagongshe.com/de/reaction/465612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoacetonitrileHCID 11534—
Edukt4-Acetylbutyric acidHCID 18407—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-Cyano-5-oxoheptanoic acidHCID 14986712—

Reaktionsschritte

To a solution of potassium hexamethyldisilazide (66 ml, 60 mmol) in dry tetrahydrofuran (140 ml) at -70° is added slowly 5-oxohexanoic acid (36 ml, 30 mmol). The resulting yellow suspension is stirred at -70° for 1 h and bromoacetonitrile (2.2 ml, 32 mmol) is added slowly. The reaction mixture is stirred at -70° for 1 h and then at room temperature for 0.5 h. The reaction is quenched by addition of 1N aqueous hydrochloric acid (100 ml). The aqueous layer is extracted twice with ether. Combined organic layer is dried, filtered and evaporated to obtain a dark oil which is purified by silica gel chromatography using 9:1 ether/hexane with 1% acetic acid as eluent to give 7-cyano-5-oxoheptanoic acid as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05153214
Quelldatensatzuspto-grants-1992_10
ORD IDord-8b89643d0bdd44568e4cd81cca446028
Quellennotizuspto-grants-1992_10