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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403282Generated: October 31, 2026

Trifluoroacetic acid → HCID 68325525, compound

https://huagongshe.com/reaction/2403282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68325408HCID 68325408—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 68325525HCID 6832552527%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of trifluoroacetic acid (51.3 μl) in water (4 ml) was added a solution of (S)-2-{4-[(4-chloro-phenyl)-methyl-amino]-phenyl}-morpholine-4-carboxylic acid tert-butyl ester (45 mg) in acetonitrile (2 ml). The reaction mixture was then capped and the mixture was shaken at 80° C. for 2 h. The reaction mixture was then cooled to room temperature and poured into 1 M aq. NaOH and the resulting mixture was extracted twice with EtOAc. The organic layers were dried over Na2SO4 and concentrated in vacuo. The crude material was purified by flash column chromatography (Isolute® Flash-NH2 from Separtis; gradient: 0% to 100% EtOAc in heptane, then 0% to 10% MeOH in EtOAc) to afford (4-chloro-phenyl)-methyl-((S)-4-morpholin-2-yl-phenyl)-amine (9 mg, 27%) as a colourless gum. MS (ISP): 305.3 ([{37Cl}M+H]+), 303.3 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-d45118dd790d4c3888eef1ffe599b0ef
Source noteuspto-grants-2014_08