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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623178Generated: October 29, 2026

Phenolphthalein → HCID 20071851, compound

https://huagongshe.com/reaction/623178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolphthaleinHCID 4764—
ReactantAcrylic AcidHCID 6581—
ReactantHCID 12986410HCID 12986410—
SolventMethanolHCID 887—
ProductHCID 20071851HCID 20071851—

Reaction Steps

The AgOH is resuspended in 400 ml of methanol. Purified tetraalkylammonium iodide (0.1 moles or 53.77 g) (Aldrich Chemical Co., Milwaukee, WI) is dissolved separately in 100 ml. of methanol and is 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 tetraheptylammonium 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 tetraheptylammonium acrylate. The resulting tetraheptylammonium acrylate was found to be electrically conductive.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04774029
Source datasetuspto-grants-1988_09
ORD IDord-1753625ade0a4f5181843f3d8f653a6d
Source noteuspto-grants-1988_09