HuagongsheHuagongshe Chemistry Print Report · For research reference only
Terephthalic Acid → HCID 21225151, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Terephthalic Acid | HCID 7489 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | HCID 11977441 | HCID 11977441 | — |
| Product | HCID 21225151 | HCID 21225151 | — |
Reaction Steps
The procedure was the same as described above for bis(tetrabutylammonium) terephthalate using 0.277 g (1.67×10-3 mol) of terephthalic acid and benzyltrimethylammonium hydroxide (3.4 mL, 0.57 g, 3.6×10-3 mol) (40% by weight in methanol). The yield of salt obtained after removal of solvent was 0.688 g, 88%. 1H and 13C NMR spectra (FIGS. 47 and 48) of the salt in D2O were obtained and are in accord with the expected structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05451643 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-d95be851ca52426fa170aa9b1281ce08 |
| Source note | uspto-grants-1995_09 |