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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242753Generated: October 27, 2026

Ethyl trifluoroacetate → N-(3-(3-bromophenyl)-3-hydroxypropyl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/242753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant3-Amino-1-(3-bromophenyl)propan-1-olHCID 57608334—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-(3-bromophenyl)-3-hydroxypropyl)-2,2,2-trifluoroacetamideHCID 57608426—

Reaction Steps

To a solution of 3-amino-1-(3-bromophenyl)propan-1-ol (146) (2.30 g, 10 mmol) in anhydrous THF (20 mL) was added ethyl trifluoroacetate (4.0 mL, 33.5 mmol). The reaction mixture was stirred at room temperature for 3 h, then concentrated under reduced pressure. Purification by column chromatography (10 to 70% EtOAc-hexanes gradient) gave N-(3-(3-bromophenyl)-3-hydroxypropyl)-2,2,2-trifluoroacetamide (147) as an oil containing ˜15% of 2,2,2-trifluoro-N-(3-hydroxy-3-phenylpropyl)acetamide. Yield (1.96 g, 60%): 1H NMR (400 MHz, DMSO-d6) δ 9.33 (s, 1H), 7.51 (t, J=2.0 Hz, 1H), 7.41 (dt, J=7.6, 2.0 Hz, 1H), 7.25-7.32 (m, 2H), 5.46 (d, J=6.4 Hz, 1H), 4.55-4.60 (m, 1H), 3.20-3.23 (m, 2H), 1.75-1.82 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653142B2
Source datasetuspto-grants-2014_02
ORD IDord-8ffec6a387fc4bd0a5ad64dc5f8458bb
Source noteuspto-grants-2014_02