HCID 20297299, compound → HCID 20297297, compound

HRID 1389695Notes

Reaction equation

HRID 1389695 reaction equation
[CH2:1]([NH:9][C:10]1[CH:11]=[C:12]([C:19]([OH:21])=[O:20])[CH:13]=[C:14]([CH:18]=1)[C:15]([OH:17])=[O:16])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:22](NC1C=C(C(O)=O)C=C(C=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=C(C=1)C(O)=O)CCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCC.CC(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCCCCC.CC(C)CCCCCCCCCCCCCNC1C=C(C(O)=O)C=C(C=1)C(O)=O.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C=C(C=1)C(O)=O)CCCCCCCCCCCCCCCCCC>>[CH2:1]([NH:9][C:10]1[CH:11]=[C:12]([C:19]([OH:21])=[O:20])[CH:13]=[C:14]([CH:18]=1)[C:15]([OH:17])=[O:16])[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 dimethyl alkylaminoisophthalates in Example 8 provide: 5-octylaminoisophthalic acid, 5-nonylaminoisophthalic acid, 5-decylaminoisophthalic acid, 5-undecylaminoisophthalic acid, 5-dodecylaminoisophthalic acid, 5-(1-methylundecyl)aminoisophthalic acid, 5-tridecylaminoisophthalic acid, 5-tetradecylaminoisophthalic acid, 5-pentadecylaminoisophthalic acid, 5-(14-methylpentadecyl)aminoisophthalic acid, 5-heptadecylaminoisophthalic acid, 5-octadecylaminoisophthalic acid, and 5-nonadecylaminoisophthalic acid.

Sources & evidence

ORD record
ord-a0cea8679e804429998a38d6ac2ee4b8
Source dataset
uspto-grants-1981_01
Patent number
US04245120

Reaction notes

Loading…