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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium trifluoroacetate | HCID 2724268 | — |
| Reactant | N-(2-oxo-2-phenylethyl)-4-(phenylmethyl)-2-morpholinecarboxamide | HCID 66990711 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Phenyl-1H-imidazol-2-yl)-4-(phenylmethyl)morpholine | HCID 178420319 | 112.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697685B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-d72d6e100ac74509a3ec4e5c9b8fd2a1 |
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| Source note | uspto-grants-2014_04 |
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