Water → HCID 67388542, compound

HRID 2261505Notes

Reaction equation

HRID 2261505 reaction equation
[NH:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.CCO[Si](OCC)(OCC)OCC.O.[NH2:20][CH2:21][CH2:22][CH2:23][Si:24]([O:31][CH2:32][CH3:33])([O:28][CH2:29][CH3:30])[O:25][CH2:26][CH3:27].CC(=O)CCC(=O)C>C1(C)C=CC=CC=1>[NH:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[CH2:29]([O:28][Si:24]([O:31][CH2:32][CH3:33])([O:25][CH2:26][CH3:27])[CH2:23][CH2:22][CH2:21][NH2:20])[CH3:30]

Participants

6

Procedure

(Pyrrole-TEOS) To a 500 mL 3-neck round bottom flask equipped with a stirbar was added 30.8 g (10× the amount of water generated by the reaction by weight) of 5 Å molecular sieves. The flask was then equipped with a reflux condenser and the remaining necks were sealed with rubber septa. The reaction flask was evacuated and backfilled with dry nitrogen three times. After the final backfill cycle, 18.9 g (85.4 mmol) of 3-aminopropyltriethoxysilane was added to the flask, along with 40 mL of anhydrous toluene. With rapid stirring, 10.8 mL (89.7 mmol) of 2,5-hexanedione was added dropwise via syringe. The contents were heated to reflux and stirred under nitrogen overnight. After an overnight stir, the contents were filtered. The filtrate was filtered a second time and collected. The collected filtrate was concentrated via rotary evaporation to yield an orange liquid (23.7 g, 94%). This solid was isolated in >98% purity, as characterized by 1H NMR spectroscopy and was not purified further. 1H NMR (CDCl3, 400 MHz): 0.65 (m, 2H); 1.23 (m, 9H); 1.75 (m, 2H); 2.23 (s, 6H) 3.77 (m, 2H); 3.84 (m, 6H); 5.76 (s, 2H). 13C NMR (CDCl3, 100 MHz): 7.64; 12.43; 18.26; 24.38; 45.99; 58.42; 104.91; 127.28.

Workup

  1. customgenerated by the reaction by weight) of 5 Å molecular sieves
  2. customThe flask was then equipped with a reflux condenser
  3. customthe remaining necks were sealed with rubber septa
  4. customThe reaction flask was evacuated
  5. temperatureThe contents were heated
  6. temperatureto reflux
  7. stirringAfter an overnight stir
  8. filtrationthe contents were filtered
  9. filtrationThe filtrate was filtered a second time
  10. customcollected
  11. concentrationThe collected filtrate was concentrated via rotary evaporation

Sources & evidence

ORD record
ord-0a3c6b06ce0a4e21b7b1633080454de6
Source dataset
uspto-grants-2010_12
Patent number
US07847048B2

Reaction notes

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