Sulfur Dioxide → HCID 131731886, compound

HRID 80281Notes

Reaction equation

HRID 80281 reaction equation
[ClH:1].[CH2:2]([CH:5]([CH2:8][CH:9]=[CH2:10])[NH:6][CH3:7])[CH:3]=[CH2:4].[S:11](=[O:13])=[O:12].CC(N=NC(C#N)(C)C)(C#N)C>CO>[ClH:1].[CH2:2]([CH:5]([CH2:8][CH:9]=[CH2:10])[NH:6][CH3:7])[CH:3]=[CH2:4].[S:11](=[O:13])=[O:12]

Participants

5

Procedure

Into a 300 ml-four-necked flask equipped with a stirrer, a thermometer, and a reflux condenser, a 1 mol/L diallyldimethylamine hydrochloride/diemthylsulfoxide (100 ml) and a 1 mol/L sulfur dioxide/diemthylsulfoxide solution (100 ml) were added and mixed, and azobis-isobutylonitrile (0.82 g) was added as a polymerization initiator to the mixture, followed by polymerizing at 40° C. for 24 hours. The reaction solution was added dropwise to methanol to precipitate the copolymer, filtered through a glass filter, followed by drying under reduced pressure, thereby obtaining 18 g of a copolymerized polymer (Production Example A-4). A weight average molecular weight of the copolymer determined by GPC (Gel Permeation Chromatography) (polyethylene glycol used as a standard) was about 3,000. The repeating unit of this polymer gas the following formula.

Workup

  1. customInto a 300 ml-four-necked flask equipped with a stirrer
  2. additionmixed
  3. customfollowed by polymerizing at 40° C. for 24 hours
  4. customto precipitate the copolymer
  5. filtrationfiltered through a glass
  6. filtrationfilter
  7. customby drying under reduced pressure

Sources & evidence

ORD record
ord-eeee6c751c7840569337c559a09db0a4
Source dataset
uspto-grants-2014_09
Patent number
US08845800B2

Reaction notes

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