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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2061784Erstellt: 26. Oktober 2026

Chloroform → 9-Allylcarbazole

https://huagongshe.com/reaction/2061784

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktCarbazoleHCID 6854—
EduktAllyl bromideHCID 7841—
EduktPotassium HydroxideHCID 14797—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt9-AllylcarbazoleHCID 3090393100%

Reaktionsschritte

Carbazole (10.1 g, 0.057 mol) and potassium hydroxide (88% wt pellets, crushed, 7.1 g, 0.11 mol) were stirred in 100 mL DMSO at 50° C. for 30 min before dropwise addition of allyl bromide (14.7 g, 0.118 mol). After 15 min the reaction mixture was poured into a 500 mL separatory funnel containing 100 mL chloroform and washed 5 times with 200 mL water to give, after solvent evaporation at 60° C. under reduced pressure, compound 15 in >99% purity as a dark brown, viscous syrup which solidified upon cooling (11.9 g, 0.057 mol, 100% yield). 1H NMR (300 MHz, CDCl3): δ=8.14-8.06 (m, 2 carbazole H), 7.49-7.32 (m, 4 carbazole H), 7.28-7.19 (m, 2 carbazole H), 6.04-5.90 (m, CH═CH2), 5.19-5.10 (m, Z-HCH═CH), 5.07-4.97 (m, E-HCH═CH), 4.92-4.85 (m, NCH2). 13C NMR (300 MHz, CDCl3): δ=140.34, 132.27, 125.67, 122.90, 120.33, 119.00, 116.74, 108.74, 45.21.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08283438B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-6bb917780b754dc9afb9efe31616f4bc
Quellennotizuspto-grants-2012_10