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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964759Generated: October 30, 2026

Benzene → HCID 54450319, compound

https://huagongshe.com/reaction/1964759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
Reactant4-ChlorobenzaldehydeHCID 7726—
Reactant1-MorpholinocyclopenteneHCID 70294—
ProductHCID 54450319HCID 5445031966.3%

Reaction Conditions

Temperature30 °C

Reaction Steps

With reflux device installed, 36.8 g (0.24 mol) of N-cyclopentenyl morpholine, 28.1 g (0.20 mol) of p-chlorobenzaldehyde and 200 mL of benzene were added to a round bottom flask and heated under reflux for 20 h. The resulting solution was cooled to 30° C., and slowly stirred while 62 mL of hydrochloric acid (6 mol/L) was added. After stirring for 2 h at room temperature, the benzene layer was separated and washed with water to neutral, and dried over anhydrous sodium sulfate overnight. Then the mixture was filtered to remove anhydrous sodium sulfate, and benzene was recovered by evaporation under reduced pressure. The residue was cooled and solidified, then recrystallized in 95% ethanol to yield 32.9 g of light yellow flaky crystal product with a yield of 66.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415505B2
Source datasetuspto-grants-2013_04
ORD IDord-8f707392f0854b7a94d64980b4d2fd92
Source noteuspto-grants-2013_04