HCID 20297296, compound → HCID 20297292, compound

HRID 1389705Notes

Reaction equation

HRID 1389705 reaction equation
[CH2:1]([NH:9][C:10]1[CH:11]=[C:12]([C:19]([OH:21])=[O:20])[C:13](=[CH:17][CH:18]=1)[C:14]([OH:16])=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:22](NC1C=C(C(O)=O)C(=CC=1)C(O)=O)[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]C.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCC.CC(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCCCCC.CC(C)CCCCCCCCCCCCCNC1C=C(C(O)=O)C(=CC=1)C(O)=O.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(=CC=1)C(O)=O)CCCCCCCCCCCCCCCCCC>>[CH2:1]([NH:9][C:10]1[CH:11]=[C:12]([C:19]([OH:21])=[O:20])[C:13](=[CH:17][CH:18]=1)[C:14]([OH:16])=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]

Participants

14

Procedure

Similarly, the diethyl 4-alkylaminophthalates described in Example 11 give, respectively, 4-octylaminophthalic acid, 4-nonylaminophthalic acid, 4-decylaminophthalic acid, 4-undecylaminophthalic acid, 4-(1-methylundecyl)aminophthalic acid, 4-dodecylaminophthalic acid, 4-tridecylaminophthalic acid, 4-tetradecylaminophthalic acid, 4-pentadecylaminophthalic acid, 4-(14-methylpentadecyl)aminophthalic acid, 4-heptadecylaminophthalic acid, 4-octadecylaminophthalic acid, and 4-nonadecylaminophthalic acid.

Workup

  1. customgive

Sources & evidence

ORD record
ord-fb8a65443c9a47b19feea923bc361b6e
Source dataset
uspto-grants-1981_01
Patent number
US04245119

Reaction notes

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