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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680449Generated: October 29, 2026

Benzene → HCID 12640216, compound

https://huagongshe.com/reaction/1680449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantMethyl 5-aminopyridine-2-carboxylateHCID 12457877—
SolventWaterHCID 962—
ProductHCID 12640216HCID 12640216—

Reaction Steps

The starting material is prepared as follows: the mixture of 30.44 g of 5-aminopyridine-2-carboxylic acid methyl ester, 30.9 g of m-chlorobenzaldehyde, and 400 ml of benzene is refluxed for 3 days on a water-separating trap. The initial suspension eventually becomes a pale yellow solution, which is evaporated. The residual yellow solid is recrystallized from benzene-ethyl acetate-diethyl ether, to yield the 5-(m-chlorobenzylideneamino)-pyridine-2-carboxylic acid methyl ester melting at 139°-142°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273779
Source datasetuspto-grants-1981_06
ORD IDord-8bcc0ee4fbdc4441a9a9e3dd765e054d
Source noteuspto-grants-1981_06