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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29168Erstellt: 23. Oktober 2026

Cyclohexyl bromide → N-cyclohexyloxyphthalimide

https://huagongshe.com/de/reaction/29168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexyl bromideHCID 7960—
EduktN-HydroxyphthalimideHCID 10665—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-cyclohexyloxyphthalimideHCID 10467039—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

N-hydroxylphthalimide (61.3 mmol, 10.0 g) was dissolved in anhydrous DMF (60 mL) under nitrogen. To the stirring solution, DBU (92.0 mmol, 13.75 mL) was injected followed by cyclohexyl bromide (76.6 mmol, 9.43 mL) and the reaction was warmed to 55° C. After stirring for 15 hours, the reaction was warmed to 80° C. for 5 hours, then cooled to room temperature and concentrated to a red oil. The reaction was partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N NaOH, brine and dried over magnesium sulfate. The solvent was removed under vacuum and the crude product was triturated with hexanes providing 2.89 g (19%) of a yellow solid. Rf: 0.7 (2:1 hexanes/ethyl acetate); H1-NMR (CDCl3): δ 7.80 (2H,m), 7.73(2H,m), 4.21 (1H,m), 2.02-1.98 (2H,m), 1.87-1.82 (2H,m), 1.59-1.53 (4H,m), 1.30-1.24 (2H,m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419967B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-16dd12d525704f8bb2157302ec748a15
Quellennotizuspto-grants-2008_09