HCID 70560377, compound → HCID 44279725, compound

HRID 1389693Notes

Reaction equation

HRID 1389693 reaction equation
[Na+:1].[Na+].[Na+].[CH2:4]([NH:12][C:13]1[CH:14]=[C:15]([C:25]([O-:27])=[O:26])[C:16]([C:22]([O-:24])=[O:23])=[C:17]([C:19]([O-:21])=[O:20])[CH:18]=1)[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[Na+].[Na+].[Na+].[CH2:31](NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)[CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38]C.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCC.[Na+].[Na+].[Na+].CC(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCCCCC.[Na+].[Na+].[Na+].CC(C)CCCCCCCCCCCCCNC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCCCCCCCC.[Na+].[Na+].[Na+].C(NC1C=C(C([O-])=O)C(C([O-])=O)=C(C([O-])=O)C=1)CCCCCCCCCCCCCCCCCC>>[Na+:1].[Na+:1].[Na+:1].[CH2:4]([NH:12][C:13]1[CH:18]=[C:17]([C:19]([O-:21])=[O:20])[C:16]([C:22]([O-:24])=[O:23])=[C:15]([C:25]([O-:27])=[O:26])[CH:14]=1)[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38]

Participants

14

Reactant 13

HCID 70560377HCID 70560377, compoundHCID 70560877HCID 70560877, compoundHCID 70561119HCID 70561119, compoundHCID 70561190HCID 70561190, compoundHCID 70561627HCID 70561627, compoundHCID 70561645HCID 70561645, compoundHCID 70562267HCID 70562267, compoundHCID 70562284HCID 70562284, compoundHCID 70562292HCID 70562292, compoundHCID 70562511HCID 70562511, compoundHCID 70562538HCID 70562538, compoundHCID 70562799HCID 70562799, compoundHCID 70562962HCID 70562962, compound

Product 1

HCID 44279725HCID 44279725, compound

Procedure

Similarly, the 5-alkylamino-1,2,3-benzenetricarboxylic acids described in Example 6 give, respectively, 5-octylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-nonylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-decylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-undecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-(1-methylundecyl)amino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-dodecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-tridecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-tetradecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-pentadecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-(14-methylpentadecyl)amino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-heptadecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, 5-octadecylamino-1,2,3-benzenetricarboxylic acid trisodium salt, and 5-nonadecylamino-1,2,3-benzenetricarboxylic acid trisodium salt.

Workup

  1. customgive

Sources & evidence

ORD record
ord-f45b4be285d34b9989e0f4271397a079
Source dataset
uspto-grants-1981_01
Patent number
US04245120

Reaction notes

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