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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367351Generated: October 27, 2026

Ammonium trifluoroacetate → 2-(4-Phenyl-1H-imidazol-2-yl)-4-(phenylmethyl)morpholine

https://huagongshe.com/reaction/2367351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium trifluoroacetateHCID 2724268—
ReactantN-(2-oxo-2-phenylethyl)-4-(phenylmethyl)-2-morpholinecarboxamideHCID 66990711—
SolventWaterHCID 962—
Product2-(4-Phenyl-1H-imidazol-2-yl)-4-(phenylmethyl)morpholineHCID 178420319112.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of N-(2-oxo-2-phenylethyl)-4-(phenylmethyl)-2-morpholinecarboxamide (850 mg, 2.51 mmol) and ammonium trifluoroacetate (1317 mg, 10.05 mmol) was heated at 150° C. under microwave condition with stirring for 1 hour. Water (150 mL) was added to the residue, and extracted with EtOAc (200 mL). The organic layer was dried (Na2SO4), filtered, and concentrated to afford the crude title compound (1.3 g) as a brown oil. This material was combined with another batch of crude title compound (250 mg) and purified by silica gel chromatography using as eluent EtOAc (1600 mL) in hexanes (400 mL) to afford the title compound (900 mg, 2.82 mmol) as a brown solid. LC-MS (ES) m/z=320 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-d72d6e100ac74509a3ec4e5c9b8fd2a1
Source noteuspto-grants-2014_04