Iodine → 1,2-Bis(trimethylsilyl)benzene
Reaction equation
[Mg].CN(C)P(N(C)C)(N(C)C)=O.Cl[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1Cl.II.Cl[Si:24]([CH3:27])([CH3:26])[CH3:25].C([O-])(O)=O.[Na+]>>[CH3:25][Si:24]([CH3:27])([CH3:26])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[Si:24]([CH3:27])([CH3:26])[CH3:25]Participants
Conditions
- Temperature
- 70 °C
Procedure
Magnesium (9.72 g, 400 mmol), hexamethylphosphoramide (HMPA) (80 mL, 460 mmol), 1,2-dichlorobenzene (14.76 g, 100 mmol), and a catalytic amount of I2 were combined in a 500 mL round bottomed flask and heated to 70° C. with stirring. Chlorotrimethylsilane was added dropwise to the solution at 70° C. The solution was stirred for an additional 30 minutes and then heated to 100° C. for 48 h. After cooling, the reaction mixture was poured over ice and NaHCO3. The Mg and precipitate were filtered off and the filtrate was extracted with ether (3×, 200 mL). The organic phase was washed with water (2×, 400 mL) and brine (1×, 400 mL) and dried with Na2SO4 and concentrated. The product was distilled under reduced pressure at 128-133° C. to yield a light yellow oil (12.0426 g, 54.13%). 1H NMR (300 MHz, CDCl3) δ 7.85 (dd, 2H, J=3.4 Hz, J=5.5 Hz, ArH), 7.49 (dd, 2H, J=3.4 Hz, J=5.5 Hz, ArH), 0.55 (s, 18H, CH3); 13C NMR (300 MHz, CDCl3) δ 145.98, 135.17, 127.76, 1.96
Workup
- stirringThe solution was stirred for an additional 30 minutes
- temperatureheated to 100° C. for 48 h
- temperatureAfter cooling
- filtrationThe Mg and precipitate were filtered off
- extractionthe filtrate was extracted with ether (3×, 200 mL)
- washThe organic phase was washed with water (2×, 400 mL) and brine (1×, 400 mL)
- dry with materialdried with Na2SO4
- concentrationconcentrated
- distillationThe product was distilled under reduced pressure at 128-133° C.
Sources & evidence
- ORD record
- ord-664d4993e8a04590bb166a9024842222
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969622B2
Reaction notes
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