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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616418Generated: November 1, 2026

5-Aminoisophthalic acid → Isophthalic Acid

https://huagongshe.com/reaction/616418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminoisophthalic acidHCID 66833—
CatalystSalicylaldehydeHCID 6998—
CatalystTributylamineHCID 7622—
ProductIsophthalic AcidHCID 8496—

Reaction Steps

53 g (0.32 mol) of isophthalic acid, 53 g (0.27 mol) of trimellitic anhydride, 3 g (0.01 mol) of an azomethine obtained by reaction of 5-amino-isophthalic acid with salicylaldehyde, 0.85 g of tributylamine as catalyst, 196 g (0.7 mol) of 3.3'-dimethyl-4,4'-di-isocyanato-diphenylmethane and 700 g of N-methylprrolidone are stirred for 6 hours at 80° C. Subsequently, 43 g (0.1 mol) of 4,4'-bis-(ethoxalylamino)-diphenylmethane are stirred into the above mixture. The temperature is then raised to 195°C, and agitation is continued for a further 6 hours at this temperature. The fluorocarbon wax suspension as described in Example 2 is added to the trion resin solution so obtained in the same weight ratio.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04074007
Source datasetuspto-grants-1978_02
ORD IDord-401b7082671f4f43861abe4678ee0689
Source noteuspto-grants-1978_02