HCID 70560309, compound → HCID 44279561, compound

HRID 1389706Notes

Reaction equation

HRID 1389706 reaction equation
[Na+:1].[Na+].[CH2:3]([NH:11][C:12]1[CH:13]=[C:14]([C:21]([O-:23])=[O:22])[C:15](=[CH:19][CH:20]=1)[C:16]([O-:18])=[O:17])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[Na+].[Na+].[CH2:26](NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]C.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCC.[Na+].[Na+].CC(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCCCCC.[Na+].[Na+].CC(C)CCCCCCCCCCCCCNC1C=C(C([O-])=O)C(=CC=1)C([O-])=O.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCCCCCCCC.[Na+].[Na+].C(NC1C=C(C([O-])=O)C(=CC=1)C([O-])=O)CCCCCCCCCCCCCCCCCC>>[Na+:1].[Na+:1].[CH2:3]([NH:11][C:12]1[CH:13]=[C:14]([C:21]([O-:23])=[O:22])[C:15](=[CH:19][CH:20]=1)[C:16]([O-:18])=[O:17])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]

Participants

14

Reactant 13

HCID 70560309HCID 70560309, compoundHCID 70560340HCID 70560340, compoundHCID 70560859HCID 70560859, compoundHCID 70561780HCID 70561780, compoundHCID 70561815HCID 70561815, compoundHCID 70561844HCID 70561844, compoundHCID 70562474HCID 70562474, compoundHCID 70562640HCID 70562640, compoundHCID 70563048HCID 70563048, compoundHCID 70563059HCID 70563059, compoundHCID 70563409HCID 70563409, compoundHCID 70563592HCID 70563592, compoundHCID 70563594HCID 70563594, compound

Product 1

HCID 44279561HCID 44279561, compound

Procedure

Similarly, the 4-alkylaminophthalic acids described in Example 12 give, respectively, 4-octylaminophthalic acid disodium salt, 4-nonylaminophthalic acid disodium salt, 4-decylaminophthalic acid disodium salt, 4-undecylaminophthalic acid disodium salt, 4-(1-methylundecyl)aminophthalic acid disodium salt, 4-dodecylaminophthalic acid disodium salt, 4-tridecylaminophthalic acid disodium salt, 4-tetradecylaminophthalic acid disodium salt, 4-pentadecylaminophthalic acid disodium salt, 4-(14-methylpentadecyl)aminophthalic acid disodium salt, 4-heptadecylaminophthalic acid disodium salt, 4-octadecylaminophthalic acid disodium salt, and 4-nonadecylaminophthalic acid disodium salt.

Workup

  1. customgive

Sources & evidence

ORD record
ord-f733758a21d84a0cb653527cde1f58f8
Source dataset
uspto-grants-1981_01
Patent number
US04245119

Reaction notes

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