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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296078Generated: October 31, 2026

Sulfuric Acid → HCID 86041032, compound

https://huagongshe.com/reaction/1296078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBenzophenoneHCID 3102—
ReactantTetraethoxysilaneHCID 6517—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Bromo-2,6-diisopropylanilineHCID 11780114—
ProductHCID 86041032HCID 8604103277%

Reaction Conditions

Temperature160 °C

Reaction Steps

40.7 g (0.195 mol) of tetraethoxysilane and 0.5 mL of sulfuric acid were added to a flask equipped with a distiller, containing 43.9 g (0.169 mol) of 4-bromo-2,6-diisopropylaniline and 24.8 g (0.130 mol) of benzophenone under a nitrogen atmosphere. The mixture was reacted by heating at 160° C. for 2 days while removing formed ethanol using the distiller. After the reaction, the resultant product was cooled to room temperature. Then, 200 mL of 1.0 M aqueous solution of potassium hydroxide was added to the resultant product and stirred for 10 minutes to obtain yellow precipitates. The obtained precipitates were filtered off and dissolved in 300 mL of ethyl acetate, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain a yellow solid. Then, the yellow solid was recrystallized in hexane at −20° C. to obtain 42 g of N-diphenylmethylene-2,6-diisopropyl-4-bromoaniline compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244805B2
Source datasetuspto-grants-2007_07
ORD IDord-776327b8ccd34d389d74d57c5e9938ab
Source noteuspto-grants-2007_07