Ethylene Glycol → Urea Urethane

HRID 2225023Notes

Reaction equation

HRID 2225023 reaction equation
[CH2:1]([OH:4])[CH2:2]O.C([N:7](CC)CC)C.C1C(CC2C=CC([N:25]=[C:26]=[O:27])=CC=2)=CC=C([N:28]=[C:29]=[O:30])C=1.C(O)C>CN1CCCC1=O>[NH2:25][C:26]([O:4][CH2:1][CH3:2])=[O:27].[NH2:7][C:29]([NH2:28])=[O:30]

Participants

6

Procedure

In an argon atmosphere, ethylene glycol (0.28 ml, 4.95 mmol) and triethylamine (0.5 ml) were dissolved in dry N-methylpyrrolidinone (5.0 ml) in a three-necked flask to give a solution. At room temperature, a solution of 4,4′-diphenylmethane diisocyanate (1.37 g, 5.50 mmol) in dry N-methylpyrrolidinone (5.0 ml) was slowly added dropwise to the solution. After the completion of the dropwise addition, the resultant solution was stirred for 1 hour at room temperature and was combined with a solution of the compound (4) (0.20 g, 0.55 mmol) prepared in Example 1 in dry N-methylpyrrolidinone (3.0 ml). The resultant mixture solution was stirred for 2 hours at room temperature. After the reaction, the reaction solution was poured into excess ethanol to precipitate the obtained polymer. The precipitated polymer was filtered off and dried under reduced pressure to give 1.34 g of a poly(urethane-urea) having a phosphorylcholine group represented by the above formula PUU-1 as light brown powder. The structure was identified by the 1H-NMR spectrum given below:

Workup

  1. customto give a solution
  2. additionAfter the completion of the dropwise addition
  3. customAfter the reaction
  4. customto precipitate the obtained polymer
  5. filtrationThe precipitated polymer was filtered off
  6. customdried under reduced pressure

Sources & evidence

ORD record
ord-af5937691017454ba9c694c26849a856
Source dataset
uspto-grants-2008_05
Patent number
US07378538B2

Reaction notes

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