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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757467Generated: November 2, 2026

Pyridine → HCID 19387978, compound

https://huagongshe.com/reaction/1757467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHexaneHCID 8058—
Reactant4-Methoxy-2-nitroanilineHCID 66793—
Reactant3-(1-Adamantyl)-4-methoxybenzoyl chlorideHCID 10804497—
SolventDichloromethaneHCID 6344—
ProductHCID 19387978HCID 1938797890%

Reaction Steps

5.38 g (32 mM) of 2-nitro-4-methoxyaniline and 50 ml of pyridine are introduced into a round-bottomed flask. 9.7 g (32 mM) of 3-(1-adamantyl)-4-methoxybenzoic acid chloride, dissolved in 100 ml of dichloromethane, are then added dropwise. At the end of addition, the mixture is brought to reflux for 12 hours. After having cooled, 100 ml of hexane are added and the precipitate obtained is recovered by filtration and washed with a mixture containing 10% ether and 90% hexane and then with water. After drying, there are obtained 12.5 g (89%) of the expected product. M.p.=208°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446059
Source datasetuspto-grants-1995_08
ORD IDord-f9427406183344daad751446e5c02efc
Source noteuspto-grants-1995_08