反応 #1884948
ord-430a39f084344f4cab3af2b7f7ac5818
反応方程式
反応条件
後処理
- 1その他The mixture was purged with argon for 10 minutes
- 2workup.ADDITIONfollowed by the slow addition of solid potassium hydroxide (2 g)
- 3workup.ADDITIONThe mixture was then poured into de-ionized water (150 mL)
- 4抽出the organic phase extracted with diethyl ether (4×100 mL)
- 5その他The organic phases were collected
- 6洗浄washed with brine (100 mL)
- 7乾燥The organic phase was dried over magnesium sulphate
- 8ろ過filtered
- 9濃縮concentrated
- 10その他to give the crude product as yellow oil
- 11その他Purification via flash chromatography with hexanes (monitored at 254 nm, collected at 320 nm)
- 12その他drying under high vacuum for 48 hours
- 13その他gave pure product as colorless oil
実験手順
To a solution of 4H-Cyclopenta[2,1-b:3,4-b′]dithiophene (CDT) (1.63 g, 9.14 mmol) in dimethyl sulfoxide (50 mL) was added hexyl bromide (3.1 g, 18.9 mmol) and a catalytic amount of potassium iodide (50 mg). The mixture was purged with argon for 10 minutes followed by the slow addition of solid potassium hydroxide (2 g). The now dark green mixture was stirred in the dark at room temperature for 72 hours. The mixture was then poured into de-ionized water (150 mL) and the organic phase extracted with diethyl ether (4×100 mL). The organic phases were collected and washed with brine (100 mL) and a saturated ammonium chloride solution (100 mL). The organic phase was dried over magnesium sulphate, filtered, and concentrated to give the crude product as yellow oil. Purification via flash chromatography with hexanes (monitored at 254 nm, collected at 320 nm) and drying under high vacuum for 48 hours gave pure product as colorless oil. Yield 2.8 g (88%). 1H NMR (500 MHz, CDCl3): δ=7.15 (d, 2H, 3JH-H=5 Hz), 6.94 (d, 2H, 3JH-H=5 Hz), 1.84 (m, 4H, C—CH2), 1.19 (m, 12H, alkyl-CH2), 0.95 (m, 4H, alkyl-CH2), 0.82 (m, 6H, alkyl-CH3).