Hexane → 2,6-Bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b']dithiophene

HRID 72030Notes

Reaction equation

HRID 72030 reaction equation
[S:1]1[CH:5]=[CH:4][C:3]2=[CH:6][C:7]3[S:8][CH:9]=[CH:10][C:11]=3[CH:12]=[C:2]12.[CH2:13]([Li])[CH2:14][CH2:15][CH3:16].[CH2:18]([Sn:22](Cl)([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:23][CH2:24][CH2:25][CH3:26])[CH2:19][CH2:20][CH3:21].CC[CH2:34][CH2:35][CH2:36][CH3:37]>C1COCC1>[CH2:13]([Sn:22]([CH2:34][CH2:35][CH2:36][CH3:37])([CH2:18][CH2:19][CH2:20][CH3:21])[C:5]1[S:1][C:2]2=[CH:12][C:11]3[CH:10]=[C:9]([Sn:22]([CH2:27][CH2:28][CH2:29][CH3:30])([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:18][CH2:19][CH2:20][CH3:21])[S:8][C:7]=3[CH:6]=[C:3]2[CH:4]=1)[CH2:14][CH2:15][CH3:16]

Participants

6

Conditions

Temperature
-78 °C

Procedure

To a stirred solution of benzo[1,2-b:4,5-b′]dithiophene (820 mg, 4.3 mmol) in THF (100 mL) under argon at −78° C. was added a solution of n-butyllithium (2.5 M, 3.44 mL, 8.6 mmol). The solution was stirred at −78° C. for 30 minutes and then warmed to −20° C. for 30 minutes. Tri-n-butyltin chloride (2.34 mL, 8.6 mmol) was added and the reaction mixture was stirred at −20° C. for 30 minutes and then allowed to warm to room temperature. After 16 hours, hexane was added and the reaction was successively washed with water and brine, dried (MgSO4), concentrated and purified by flash chromatography (100% hexanes). 2,6-bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b′]dithiophene (1.4 g, 42%) was isolated along with product contaminated with the monostannylated benzodithiophene. 1H-NMR: 400 MHz, (CDCl3) δ: 8.27 (s, 2H), 7.38 (s, 2H), 1.65-1.57 (m, 12H), 1.41-1.32 (m, 12H), 1.26-1.11 (m, 12H), 0.91 (t, J=7.3 Hz, 18H) ppm.

Workup

  1. temperaturewarmed to −20° C. for 30 minutes
  2. stirringthe reaction mixture was stirred at −20° C. for 30 minutes
  3. temperatureto warm to room temperature
  4. waitAfter 16 hours
  5. washthe reaction was successively washed with water and brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. custompurified by flash chromatography (100% hexanes)

Sources & evidence

ORD record
ord-d72805000c254ff291d5fd8226d5b7a5
Source dataset
uspto-grants-2014_09
Patent number
US08822430B2

Reaction notes

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