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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710451Generated: October 29, 2026

Trifluoroacetic anhydride → N-(3-(1Admantyl)-4-isopropoxyphenethyl)-2,2,2-trifluoro-acetamide

https://huagongshe.com/reaction/710451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-(3-(1-Admantyl)-4-isopropoxyphenyl)ethanamineHCID 66726392—
ProductN-(3-(1Admantyl)-4-isopropoxyphenethyl)-2,2,2-trifluoro-acetamideHCID 8712650382.4%

Reaction Steps

To a stirred solution of 2-(3-(1-Admantyl)-4-isopropoxyphenyl)ethanamine (0.28 g, 0.86 mmol) in a mixture of solvents (CH2Cl2:Et3N: 10:0.5 ml) (CF3CO)2O (0.157 ml) was added at 0° C. under N2. The reaction mixture was stirred for 2 h at room temperature, then the solvent was evaporated to dryness. The residue was diluted to 50 ml with EtOAc and washed with 1M HCl. The organic layer was separated, dried over MgSO4 and filtered. The filtrate was evaporated to dryness to give the title product (0.29 g, 82.4%). 1H-NMR (CDCl3) 1.37 (d, 6H, J=6 Hz); 1.67-1.75 (m, 6H); 2.04-2.23 (m, 9H); 2.78 (tr, 2H, J=6.84 Hz); 3.53-3.59 (m, 2H); 4.57-4.63 (m, 1H); 6.77 (d, 1H, J=8.32 Hz); 6.92 (dd, 1H, J=2.21, 8.27 Hz); 6.98 (d, 1H, J=2.21 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181182B2
Source datasetuspto-grants-2015_11
ORD IDord-0eb14a34d4b94b729ae8c5e67395e459
Source noteuspto-grants-2015_11