Iodine → Benzylbenzene diisocyanate

HRID 45416Notes

Reaction equation

HRID 45416 reaction equation
[NH:1]([CH2:5][CH2:6]O)CCO.II.[C:10]1(=[O:16])O[C:13](=O)[CH:12]=[CH:11]1.[C:17]1([CH3:27])[CH:22]=[CH:21][C:20](S(O)(=O)=O)=[CH:19][CH:18]=1>>[N-:1]=[C:10]=[O:16].[N-:1]=[C:10]=[O:16].[C:17]1([CH2:27][C:6]2[CH:5]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

5

Reactant 4

HCID 807IodineHCID 6101p-Toluenesulfonic acidHCID 7923Maleic AnhydrideHCID 8113Diethanolamine

Product 1

HCID 19824838Benzylbenzene diisocyanate

Procedure

The above amounts of diethanolamine and iodine were added to the above amount of soybean oil with stirring. The mixture was stirred for 24 hours at a temperature between about 200° F. and about 226° F. Then, the above amounts of maleic anhydride and p-toluenesulphonic acid were added with stirring. The mixture was stirred under vacuum for 20 hours at a temperature between about 200° F. and about 226° F. to give a liquid soybean oil based polyol with a hydroxyl number of 55. A reaction mixture of about 10.00 grams of the polyol and the above indicated amount of diphenylmethane diisocyanate yielded a solid soybean oil based polyurethane material.

Workup

  1. stirringThe mixture was stirred for 24 hours at a temperature between about 200° F. and about 226° F
  2. stirringwith stirring
  3. stirringThe mixture was stirred under vacuum for 20 hours at a temperature between about 200° F. and about 226° F.
  4. customto give a liquid soybean oil

Sources & evidence

ORD record
ord-db5b6e3cb3ac4198a70bc384d870ae92
Source dataset
uspto-grants-2013_09
Patent number
US08541536B2

Reaction notes

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