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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594388Generated: November 2, 2026

Acetic Acid → HCID 69085197, compound

https://huagongshe.com/reaction/594388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant4-(Trifluoromethoxy)benzylamineHCID 571846—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 61645017HCID 61645017—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69085197HCID 69085197—

Reaction Steps

A mixture of methyl 4-oxo-4-(2,4,6-trimethoxyphenyl)butanoate (200 mg; 0.70 mmol; 1.0 equiv.), (4-(trifluoromethoxy)phenyl)methanamine (677 mg; 3.54 mmol; 5.0 equiv.), acetic acid (472 mg; 7.86 mmol; 11.1 equiv.), and NaBH3CN (93 mg; 1.41 mmol; 2.0 equiv.) in anh. THF (1.5 ml), and anh. MeOH (1.5 ml) was refluxed, under nitrogen, for 24 h. After cooling to rt, 15% aq. NaOH was added, and the organic solvents were removed under reduced pressure. The residue was extracted with DCM, and the mixed organic layers were washed with brine, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=50/1) afforded 1-(4-(trifluoromethoxy)benzyl)-5-(2,4,6-trimethoxyphenyl)pyrrolidin-2-one as a colorless oil. LC-MS (conditions D): tR=1.08 min.; [M+H]+: 425.72 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-b287521dc10d41bb846f53ac738449b8
Source noteuspto-grants-2016_01