Salicylic Acid → HCID 178524363, compound

HRID 1614715Notes

Reaction equation

HRID 1614715 reaction equation
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:11]([OH:22])(=[O:21])[C:12]1[CH:20]=[CH:19][CH:18]=[C:14]([C:15]([OH:17])=[O:16])[CH:13]=1>>[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:11]([O-:22])(=[O:21])[C:12]1[CH:20]=[CH:19][CH:18]=[C:14]([C:15]([O-:17])=[O:16])[CH:13]=1

Participants

3

Reactant 2

HCID 338Salicylic AcidHCID 8496Isophthalic Acid

Product 1

HCID 178524363HCID 178524363, compound

Conditions

Temperature
132 °C

Procedure

The procedure was repeated with 1 mole of salicylic acid and 3 moles of isophthalic acid to produce 520 g of a light colored, translucent glassy product. DSC: Tg at 100° C. (second heat), 132° C. (third heat).

Workup

  1. customto produce 520 g of a light colored, translucent glassy product

Sources & evidence

ORD record
ord-bc85ad7fa14e4b709b738fa2f98c8451
Source dataset
uspto-grants-1993_03
Patent number
US05198572

Reaction notes

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