Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165104Generated: November 1, 2026

Hydrochloric Acid → HCID 13115422, compound

https://huagongshe.com/reaction/1165104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenolHCID 996—
ReactantSulfuric AcidHCID 1118—
ReactantNitromethaneHCID 6375—
Reactant1,1,2,2-TetrachloroethaneHCID 6591—
ReactantTerephthalic AcidHCID 7489—
ReactantAluminum(III) ChlorideHCID 6451240—
ProductHCID 13115422HCID 1311542250%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a mixture formed by adding 0.4 moles of AlCl3 to 0.6 mole of sym-tetrachloroethane are sequentially added, with stirring, 0.46 mole of nitromethane, 0.2 mole of terephthalic acid (reagent grade) and gradually 0.2 mole of phenol. The initial temperature of the resulting mixture is 25° C. and the temperature is raised to about 30° C. after 2 hours, then to about 40° C. after 4 hours, and about 1 hour later or until all HCl evolution is complete, the resulting mixture is allowed to stand overnight at room temperature. The mixture is treated with dilute sulfuric acid and the sym-tetrachloroethane is distilled from the mixture. The recovered solid is redissolved in boiling 10% Na2CO3, filtered, reprecipitated with concentrated HCl, and finally washed with water. About a 50% yield of 4-(4-hydroxybenzoyl) benzoic acid of good purity is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906784
Source datasetuspto-grants-1990_03
ORD IDord-5d3f76b5ae884fa98c53516ff08dfe3e
Source noteuspto-grants-1990_03