HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623177Generated: October 29, 2026
Phenolphthalein → HCID 20071852, compound
https://huagongshe.com/reaction/623177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenolphthalein | HCID 4764 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | N,N,N-Trihexylhexan-1-aminium hydroxide | HCID 13998878 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20071852 | HCID 20071852 | — |
Reaction Steps
The AgOH is resuspended in 400 ml of methanol. The purified tetraalkylammonium iodide (0.1 moles or 48.2 g) (Aldrich Chemical Co., Milwaukee, WI) is dissolved separately in 100 ml. of methanol and added to the AgOH suspension. Almost immediately, the AgOH develops a greenish cast. The mixture is stirred for an hour and then filtered through a sintered-glass funnel. The filtrate now contains 0.1 moles of tetrahexylammonium hydroxide. A small amount of phenolphthalein is added, turning the solution red indicating that the solution is basic. Acrylic acid is added until the red color disappears. The methanol is removed by evaporation in a rotary flash evaporator leaving tetrahexylammonium acrylate. The resulting tetrahexylammonium acrylate was found to be electrically conductive.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04774029 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-f1d80aa3f95a43a9a596f5a8c3f6c8d6 |
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| Source note | uspto-grants-1988_09 |
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