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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964784Generated: October 29, 2026

Benzene → HCID 67064754, compound

https://huagongshe.com/reaction/1964784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
Reactant1-MorpholinocyclopenteneHCID 70294—
ProductHCID 67064754HCID 6706475480.2%

Reaction Conditions

Temperature30 °C

Reaction Steps

With reflux device installed, 36.8 g (0.24 mol) of N-cyclopentenyl morpholine, 0.20 mol of 3,4,5-trimethoxybenzaldehyde 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 80.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415505B2
Source datasetuspto-grants-2013_04
ORD IDord-3203c41a118d4b58816c6569ded06d7e
Source noteuspto-grants-2013_04