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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964778Generated: October 28, 2026

Benzene → HCID 67064881, compound

https://huagongshe.com/reaction/1964778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
ReactantVeratraldehydeHCID 8419—
Reactant1-MorpholinocyclopenteneHCID 70294—
ProductHCID 67064881HCID 6706488169.3%

Reaction Conditions

Temperature30 °C

Reaction Steps

With reflux device installed, 36.8 g (0.24 mol) of N-cyclopentenyl morpholine, 0.20 mol of 3,4-dimethoxybenzaldehyde and 200 mL 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 cyclohexane/ethanol to yield a light yellow flaky crystal product with a yield of 69.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415505B2
Source datasetuspto-grants-2013_04
ORD IDord-b334d22c73b74344b18c0db47975dcdb
Source noteuspto-grants-2013_04