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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560956Generated: October 25, 2026

Ethanolamine → 2-Phenyl-2-oxazoline

https://huagongshe.com/reaction/560956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantBenzonitrileHCID 7505—
ReactantCalcium ChlorideHCID 5284359—
Product2-Phenyl-2-oxazolineHCID 244030—

Reaction Steps

The methods (1) to (6) will be described more specifically. For example, as the method (1), potassium hydroxide or acetic anhydride is reacted to 2-chloroethylformamide to provide 2-oxazoline, and the case where 2-bromoethylbenzamide is used provides 2-phenyl-2-oxazoline (see, for example Non-patent Document 1). As the method (2), thionyl chloride is reacted to 2-formamide ethanol to provide 2-oxazoline, and N-(2-hydroxyethyl)benzamide is heated with phosphorous pentoxide to provide 2-phenyl-2-oxazoline (see, for example, Non-patent Document 2). As the method (3), benzoic acid and 2-aminoethanol are heated with alumina to provide 2-phenyl-2-oxazoline (see, for example, Non-patent Document 3). As the method (4), benzonitrile and 2-aminoethanol are heated with calcium chloride at 110 to 120° C. to provide 2-phenyl-2-oxazoline (see, for example, Non-patent Document 4 and Patent Document 1). As the method (5), methyl benzimidate and 2-aminoethanol are heated with alumina to provide 2-phenyl-2-oxazoline (see, for example, Non-patent Document 5). Vinylbenzamide is simply heated to provide 2-phenyl-2-oxazoline. As the method (6), N-allylbenzamide is heated with sulfuric acid to provide 5-methyl-2-phenyl-2-oxazoline (see, for example, Non-patent Document 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063205B2
Source datasetuspto-grants-2011_11
ORD IDord-d4ef88bdd5bc4d3aae218e3d93cc12d3
Source noteuspto-grants-2011_11