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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356566Generated: October 30, 2026

Terephthalic Acid → HCID 21225151, compound

https://huagongshe.com/reaction/356566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTerephthalic AcidHCID 7489—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantHCID 11977441HCID 11977441—
ProductHCID 21225151HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837381
Source datasetuspto-grants-1998_11
ORD IDord-5aae2e98c2104e27be14f75aace67f6a
Source noteuspto-grants-1998_11