Water → HCID 86742621, compound
Reaction equation
C(O)[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)[OH:3].[S:13](=[O:17])(=[O:16])([OH:15])[NH2:14].[NH:18]1C=CC=C1.[OH2:23]>CN(C)C=O>[NH4+:14].[S:13]([O-:15])([O-:23])(=[O:17])=[O:16].[S:13]([O-:15])([O-:3])(=[O:17])=[O:16].[S:13]([O-:15])([O-:23])(=[O:17])=[O:16].[S:13]([O-:15])([O-:23])(=[O:17])=[O:16].[S:13]([O-:15])([O-:23])(=[O:17])=[O:16].[S:13]([O-:15])([O-:23])(=[O:17])=[O:16].[NH4+:18].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14].[NH4+:14]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Mannityl hexasulfate ammonium salt is prepared from mannitol and sulfamic acid in dimethylformamide. A mixture of 5 grams of pyrrole and 1 gram of this ammonium salt is dissolved in 200 ml. of water. Utilizing the apparatus described in Example 7, the polymerization is carried out at a current of about 0.4 amperes over a period of 20 minutes. The product is a black electronically conducting film which is shiny on the substrate side and rough on the solution side.
Workup
- dissolutionis dissolved in 200 ml
- customof 20 minutes
Sources & evidence
- ORD record
- ord-ff7b7f149c9042518d015386a20e548e
- Source dataset
- uspto-grants-1988_12
- Patent number
- US04791374
Reaction notes
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