Iodoethane → 3-bromo-9-ethyl-6,7,8,9-tetrahydro-5H-carbazole

A 500-mL round-bottomed flask was charged with 3-bromo-6,7,8,9-tetrahydro-5H-carbazole (5 g, 20.08 mmol, 1.00 equiv) in N,N-dimethylformamide (270 mL). To this solution was added sodium hydride (1.2 g, 30.00 mmol, 1.50 equiv, 60%) in several batches at −10° C., followed by addition of iodoethane (6.26 g, 40.13 mmol, 2.00 equiv) as a solution in N,N-dimethylformamide (30 mL) drop wise −10° C. The resulting mixture was stirred at room temperature for 30 minutes. The reaction progress was monitored by TLC (EtOAc:PE=1:1). Upon completion, the reaction was then quenched by the addition of water/ice (120 mL). Then, the mixture was extracted with ethyl acetate (4×80 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered off and concentrated on a rotary evaporator. The residue was purified by a silica gel column chromatography eluted with ethyl acetate/petroleum ether (1/20) affording 3-bromo-9-ethyl-6,7,8,9-tetrahydro-5H-carbazole as brown oil (5 g, 90%).

1. customUpon completion, the reaction was then quenched by the addition of water/ice (120 mL)
2. extractionThen, the mixture was extracted with ethyl acetate (4×80 mL)
3. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
4. filtrationfiltered off
5. concentrationconcentrated on a rotary evaporator
6. customThe residue was purified by a silica gel column chromatography
7. washeluted with ethyl acetate/petroleum ether (1/20)

ORD record

ord-bd4faea5b35641a1b0d0f263b3ede9ee

Source dataset

uspto-grants-2011_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08080566B1