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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384282Generated: November 1, 2026

Benzaldehyde → HCID 21186745, compound

https://huagongshe.com/reaction/1384282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 21186750HCID 21186750—
CatalystZincchlorideHCID 3007855—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 21186745HCID 2118674533.4%

Reaction Steps

Ethyl 2-methyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridine-3-carboxylate (1.07 g, 4.40 mmol) and benzaldehyde (583.6 mg, 5.50 mmol) were dissolved in acetic anhydride (2.0 ml), and the solution was mixed with zinc chloride (40.0 mg, 0.30 mmol) at room temperature and then heated under reflux for 36 hours. After cooling, acetic anhydride was evaporated under reduced pressure, and the thus obtained residue was mixed with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate and then the solvent was evaporated under reduced pressure and the resulting residue was purified by a silica gel column chromatography (ether:hexane=1:6-1:5) to obtain the title compound (471.4 mg, 33.4%) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258829B1
Source datasetuspto-grants-2001_07
ORD IDord-5b670901d5d843159f95704ab0e21504
Source noteuspto-grants-2001_07