HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminoisophthalic acid → Isophthalic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminoisophthalic acid | HCID 66833 | — |
| Catalyst | Salicylaldehyde | HCID 6998 | — |
| Catalyst | Tributylamine | HCID 7622 | — |
| Product | Isophthalic Acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04074007 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-401b7082671f4f43861abe4678ee0689 |
| Source note | uspto-grants-1978_02 |