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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25667Erstellt: 24. Oktober 2026

Lactonitrile → HCID 178484853, Verbindung

https://huagongshe.com/de/reaction/25667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLactonitrileHCID 6572—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktHCID 178484846HCID 178484846—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 178484853HCID 17848485341,5%

Reaktionsschritte

To 1.0 g (2.18 mmol) trans-N-[4-(3-Bromo-propoxy)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide in 10 ml acetonitrile was added 0.29 ml (3.1 mmol) acetocyanhydrine in 5 ml acetonitrile and 0.37 ml (2.5 mmol) 1,8-Diazabicyclo-(5,4,0)-undec-7-ene in 5 ml acetonitrile. The solution was stirred at RT over night. An additonal amount of acetocyanhydrine and 1,8-Diazabicyclo-(5,4,0)-undec-7-ene were added and the solution stirred at 50° C. for 6 h. The mixture was concentrated and dissolved in water/ether. The organic phase was washed with brine, dried over Na2SO4 and was evaporated to give 366 mg (41%) trans-N-[4-(3-Cyano-propoxy)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide as light yellow oil, MS: 404 (M).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858651B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-19a319e7fabe4c418e92433f29cf6727
Quellennotizuspto-grants-2005_02