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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386183Generated: October 30, 2026

2,2,2-Trifluoro-N,N-dimethylacetamide → 7-Phenyl-1-(5-(2,2,2-trifluoroacetyl)oxazol-2-yl)heptan-1-one

https://huagongshe.com/reaction/2386183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoro-N,N-dimethylacetamideHCID 350491—
Reactant2-(1-{[tert-Butyl(dimethyl)silyl]oxy}-7-phenylheptyl)-1,3-oxazoleHCID 68523722—
Reactant1-(2-(1-(tert-Butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)-2,2,2-trifluoroethanoneHCID 68527554—
Product7-Phenyl-1-(5-(2,2,2-trifluoroacetyl)oxazol-2-yl)heptan-1-oneHCID 1199181258%

Reaction Steps

1-(2-(1-(tert-Butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)-2,2,2-trifluoroethanone. The title compound was prepared from 2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazole (100 mg, 0.268 mmol) and N,N-dimethyltrifluoroacetamide following General Procedure K. Flash chromatography (2-10% EtOAc/hexanes) yielded the title compound as a clear oil (73 mg, 58%): 1H NMR (CDCl3, 600 MHz) δ 8.01 (s, 1H), 7.28-7.26 (m, 2H), 7.18-7.16 (m, 3H), 4.90 (t, 1H, J=7.0 Hz), 2.60 (t, 2H, J=7.5 Hz), 1.96-1.88 (m, 2H), 1.63-1.60 (m, 2H), 1.44-1.35 (m, 6H), 0.90 (s, 9H), 0.09 (s, 3H), 0.01 (s, 3H); 13C NMR (CDCl3, 150 MHz) δ 172.8, 169.2 (q, J=39 Hz), 145.1, 143.5, 140.6, 1292, 129.1, 126.5, 116.6 (q, J=287 Hz), 69.5, 37.1, 36.8, 32.2, 30.0, 29.9, 26.5, 25.7, 19.1, −4.2, −4.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268817B2
Source datasetuspto-grants-2012_09
ORD IDord-c41764e756d9454b8549246d36742a1d
Source noteuspto-grants-2012_09