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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1530135Erstellt: 27. Oktober 2026

N-bromobutanimide → HCID 58095216, Verbindung

https://huagongshe.com/reaction/1530135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Eduktbeta-CyclodextrinHCID 444041—
EduktThioureaHCID 2723790—
Edukt3-(2,4-Dichlorophenyl)-3-oxopropanenitrileHCID 13630728—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
ProduktHCID 58095216HCID 5809521642%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

beta-Cyclodextrin (4.29 g, 3.78 mmol) was dissolved in water (75 mL) at 50° C. and a solution of 3-(2,4-dichlorophenyl)-3-oxopropanenitrile (810 mg, 3.8 mmol) in Acetone (3.80 mL) was added dropwise, followed by NBS (0.808 g, 4.54 mmol) and thiourea (0.346 g, 4.54 mmol). Reaction mixture was stirred at 50° C. 1 hr. LCMS indicated complete conversion. Reaction mixture was cooled to rt, extracted with ethyl acetate (3×50 mL), dried with MgSO4, filtered and concentrated under reduced pressure. The residue was purified by ISCO with 5-30% ethyl acetate in hexanes to give 0.43 g of the title compound (42%). LCMS; (FA) ES+, 270, 272, 1H NMR (400 MHz, d1-chloroform) δ 7.49 (d, J=1.84 Hz, 1H), 7.41 (d, J=8.30 Hz, 1H), 7.31 (dd, J=8.16, 1.74 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09090601B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-91725012d7174cc38e98f48532a2f06c
Quellennotizuspto-grants-2015_07