N,N'-Dimethylurea → HCID 86737268, compound

HRID 903532Notes

Reaction equation

HRID 903532 reaction equation
[C:1]1([S:7]([O-:10])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O[CH2:12][P+:13]([CH2:18]O)([CH2:16]O)[CH2:14]O.[CH3:20][NH:21][C:22]([NH:24][CH3:25])=[O:23]>C1(C)C=CC=CC=1>[C:1]1([S:7]([O-:10])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:20][N:21]([CH2:18][P+:13]([CH2:12][N:21]([CH3:20])[C:22]([NH:24][CH3:25])=[O:23])([CH2:14][N:21]([CH3:20])[C:22]([NH:24][CH3:25])=[O:23])[CH2:16][N:21]([CH3:20])[C:22]([NH:24][CH3:25])=[O:23])[C:22]([NH:24][CH3:25])=[O:23]

Participants

4

Reactant 2

HCID 7293N,N'-DimethylureaHCID 23463259HCID 23463259, compound

Product 1

HCID 86737268HCID 86737268, compoundYield 73.9%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Reaction of tetrakis(hydroxymethyl)phosphonium benzenesulfonate (15.61 g, 0.05 mol) with 1,3-dimethylurea (17.62 g, 0.2 mol) in toluene (200 ml), following Example 1, gave 21.91 g (73.9%) of tetrakis(1,3-dimethylureidomethyl)phosphonium benzenesulfonate (I, R=R'=CH3, R"=H, X=SO3C6H5) as a white, crystalline solid, mp 103°-105° C. after three recrystallizations from acetonitrile (3 ml/g). The analytical sample, dried under vacuum for 4 hr at 56° C. (acetone), analyzed as a hydrate.

Sources & evidence

ORD record
ord-c7e0079cf528446e8a4efb314d1fd79d
Source dataset
uspto-grants-1980_10
Patent number
US04228100

Reaction notes

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