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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488897Generated: November 2, 2026

Hydrochloric Acid → Phthalonitrile

https://huagongshe.com/reaction/1488897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
Reactant1,2-Benzenedicarbonitrile, 3-nitro-HCID 162652—
ReactantSodium NitriteHCID 23668193—
SolventN,N-dimethylacetamide 1-methyl-2-pyrrolidoneHCID 22717425—
ProductPhthalonitrileHCID 7042134.2%

Reaction Conditions

Temperature165 °C

Reaction Steps

In 180 ml of an N,N-dimethylacetamide/1-methyl-2-pyrrolidone (=1/1 volume ratio) mixed solvent were dissolved 30 g of 3-nitrophthalonitrile, to which 11.97 g of sodium nitrite were added. The mixture was stirred at 165° C. for 40 minutes. After being cooled to room temperature, the mixture was added with 16.8 g of potassium carbonate, which was further stirred at 150° C. for 40 minutes and thereafter cooled to 40° C. Then, 25 g of chloromethyltrimethylsilane were added dropwise. After the addition, the mixture was stirred for 28 hours while maintaining the reaction temperature at 80°-90° C. The reaction vessel was then cooled to room temperature and 350 ml of dilute hydrochloric acid was added. The mixture was extracted with 1.5 liters of toluene. The organic layer was washed well with water and water was removed with magnesium sulfate. Thereafter, toluene was removed by distillation and the residue was purified with a toluene/silica gel column to obtain 29.8 g (yield: 74.7%) of a compound having the above-described formula (XV).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677025
Source datasetuspto-grants-1997_10
ORD IDord-ead03d4903234b6a860ceaeb23f2100b
Source noteuspto-grants-1997_10