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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756886Generated: October 25, 2026

Salicylamide → 2,2-dibutyl-4-oxo-2,3-dihydro-4H-1,3-benzoxazine

https://huagongshe.com/reaction/1756886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylamideHCID 5147—
Reactant5-NonanoneHCID 10405—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
Product2,2-dibutyl-4-oxo-2,3-dihydro-4H-1,3-benzoxazineHCID 1008401792.5%

Reaction Steps

A mixture of 20 g of dibutylketone, 19.3 g of salicylamide and 2.7 g of p-toluenesulfonic acid monohydrate is added to 300 ml of toluene and the mixture is refluxed overnight by making use of a dehydrator of Dean Stark. After cooling, the reaction mixture is washed, dried and evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent; hexane:ethyl acetate =95:5) to obtain 34 g of 2,2-dibutyl-4-oxo-2,3-dihydro-4H-1,3-benzoxazine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442055
Source datasetuspto-grants-1995_08
ORD IDord-9efcac42f446489ba5cf5243c6c30bd3
Source noteuspto-grants-1995_08