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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44175Erstellt: 24. Oktober 2026

2-Bromopropane → HCID 66911305, Verbindung

https://huagongshe.com/de/reaction/44175

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromopropaneHCID 6358—
Edukt6-Bromo-3,4-dihydroquinolin-2(1H)-oneHCID 14373281—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 66911305HCID 6691130538,9%

Reaktionsschritte

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (750 mg, 3.32 mmol) in 20 ml dry DMF was added potassium tert-butylate (804 mg, 6.64 mmol). After the mixture was stirred for 30 min at room temperature, a solution of isopropyl bromide (814 mg, 6.64 mmol) in 10 ml dry DMF was added and the mixture heated to 80° C. After stirring for additional 48 h, the mixture was cooled to room temperature and diluted with 150 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 4/1, Rf=0.21) gave 6-bromo-1-isopropyl-3,4-dihydro-1H-quinolin-2-one (347 mg, 1.29 mmol, 33%) as pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541404B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-5ceeb796fc7647d8bdb01bfa4f4dd658
Quellennotizuspto-grants-2013_09