Potassium Iodide → HCID 86703812, compound

HRID 2172586Notes

Reaction equation

HRID 2172586 reaction equation
[CH2:1]([OH:10])[CH2:2][O:3][CH2:4][CH2:5][O:6][CH2:7][CH2:8][OH:9].[CH3:11][C:12](C)([O-])[CH3:13].[K+].[I-].[K+].C(Br)C=C>C1COCC1>[CH2:13]([CH:1]([OH:10])[CH2:2][O:3][CH2:4][CH2:5][O:6][CH2:7][CH2:8][OH:9])[CH:12]=[CH2:11]

Participants

6

Procedure

Allyl-triethylene glycol was prepared according to the literature method with modifications (Setz O, et al. Angew Chem Int Ed Engl. 1995, 34, 803-805). Thus, the mixture of triethylene glycol (11.83 g, 78.8 mmol), potassium t-butoxide (4.42 g, 39.4 mmol) and potassium iodide (0.65 g, 3.94 mmol) in THF (500 mL) was stirred at room temperature for 0.5 h, into which was added dropwise allyl bromide (4.767 g, 39.4 mmol) in THF (120 mL) over a period of 1.5 h. After continuing to be stirred at room temperature for 36 h, the mixture was filtered through a celite pad. The crude product, obtained after removal of solvents under vacuum, was purified by a silica gel column chromatography eluting with hexane/ethyl acetate (1:1) to afford the product (4.9 g, 25.8 mmol, 65% yield) with chemical structure confirmed by 1H NMR and MS.

Workup

  1. stirringto be stirred at room temperature for 36 h
  2. filtrationthe mixture was filtered through a celite pad
  3. customThe crude product, obtained

Sources & evidence

ORD record
ord-bab0e0382f60401da3150ecca1466b78
Source dataset
uspto-grants-2015_06
Patent number
US09056141B2

Reaction notes

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