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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734018Generated: October 27, 2026

Hydrochloric Acid → HCID 19439673, compound

https://huagongshe.com/reaction/1734018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant3-((1,3-Dioxoisoindolin-2-yl)methyl)benzonitrileHCID 12375336—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19439673HCID 1943967366%

Reaction Steps

A solution of hydrazine hydrate (4.0 g) in methanol was added dropwise to a mixture of N-(3-cyanobenzyl)phthalimide (17.0 g) in tetrahydrofuran (150 ml) and methanol (120 ml) at ambient temperature under stirring and the resultant mixture was stirred for 3 hours at ambient temperature. To the reaction mixture was added dropwise 6N-hydrochloric acid (25 ml) and the mixture was stirred for one hour at ambient temperature. The reaction mixture was evaporated in vacuo. To the residue was added water (60 ml) and the mixture was stirred at 10 minutes and filtrated. The filtrate was washed with ethyl acetate and adjusted to pH 8.0 with 20% potassium carbonate solution. Acetic anhydride (15 ml) was added dropwise to the resulting solution at 8° to 20° C. under stirring and the mixture was stirred for one hour at 10° to 20° C. The reaction mixture was extracted with ethyl acetate, and extract was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was recrystallized from a mixture of ethyl acetate and diisopropyl ether to give N-(3-cyanobenzyl)acetamide (7.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532258
Source datasetuspto-grants-1996_07
ORD IDord-58480338e0874a3b81c5d0453c97a24e
Source noteuspto-grants-1996_07