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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 511664Erstellt: 24. Oktober 2026

Isopropanol → N-(4-(Oxetan-3-YL)phenyl)acetamide

https://huagongshe.com/de/reaction/511664

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
Edukt(1R,2R)-2-AminocyclohexanolHCID 735777—
Edukt3-IodooxetaneHCID 13356686—
EduktSodium hexamethyidisilazaneHCID 45051731—
KatalysatorNickel(II) iodideHCID 26038—
LösungsmittelEthanolHCID 702—
ProduktN-(4-(Oxetan-3-YL)phenyl)acetamideHCID 67776166—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

(4-Acetamidophenyeboronic acid {670 mg, 3.7 mmol), Nickel (II) iodide (35 mg, 0.11 mmol), trans-2-aminocyclohexanol (17 mg, 0.11 mmol), and Sodium hexamethyldisilazane (690 mg, 3.7 mmol) were weighed into a microwave reaction vial. A septum was placed over the top, nitrogen was purged and Isopropyl alcohol (5.7 ml, 75 mmol) was added. The vial was purged with nitrogen for 10 minutes and 3-iodooxetane (344 mg, 1.87 mmol) was added in 0.75 ml isopropyl alcohol. The septum was replaced with a microwave vial cap and the mixture was heated in a microwave reactor (microwave conditions: CEM Discovery Explorer microwave reactor; Ramp time: 10 min; 80° C. for 30 min; power: 300 W). The crude reaction mixture was diluted with 8 ml EtOH and the suspension was filtered through a pad of solka Floc®. The pad was washed with 35 ml EtOH and the filtrate was concentrated. The crude material was purified by flash chromatography (SiO2, eluting with 40-60% EtOAc/CH2Cl2) to give the desired product as an oil (200 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096634B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-5a49b4b067894506beb19446be3ed6fc
Quellennotizuspto-grants-2015_08