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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20843Generated: October 26, 2026

Tetrabutylammonium Fluoride → (+/-)-2-Chloro-N-[{1-[(2-hydroxyethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/20843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(+)-2-Chloro-n-[{1-[(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamideHCID 59347865—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-2-Chloro-N-[{1-[(2-hydroxyethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamideHCID 59347872—

Reaction Steps

To a solution of (±)-2-chloro-N-[{1-[(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamide D30 (0.390 g; 0.685 mmol) in THF (10 ml) was added tetrabutylammonium fluoride (1M solution in THF 1.6 ml; 1.6 mmol). The reaction mixture was allowed to stir at room temperature for 4 h. The desired product was isolated by column chromatography on silica using 20% to 50% ether in n-pentane, the solvent was reduced in volume by evaporation in vacuo and loaded onto an SCX cartridge. Washing with DCM, then methanol followed by elution with 1M ammonia in methanol afforded the title product (170 mg, 73%). Mass Spectrum (Electrospray LC/MS). Found 455 (MH+). C23H2635ClF3N2O2 requires 454. Ret. time: 2.09 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745642B2
Source datasetuspto-grants-2010_06
ORD IDord-d50f960bff5b41df87c9c0d7b24ed7e1
Source noteuspto-grants-2010_06