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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014670Generated: October 31, 2026

N-Allyl-2,2,2-trifluoroacetamide → (E)-N-(3-(3-(cyclohexylmethoxy)-5-fluorophenyl)allyl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/1014670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Allyl-2,2,2-trifluoroacetamideHCID 558569—
Reactant1-Bromo-3-(cyclohexylmethoxy)-5-fluorobenzeneHCID 67317171—
SolventDimethylformamideHCID 6228—
Product(E)-N-(3-(3-(cyclohexylmethoxy)-5-fluorophenyl)allyl)-2,2,2-trifluoroacetamideHCID 86637624—

Reaction Steps

Coupling of 1-bromo-3-(cyclohexylmethoxy)-5-fluorobenzene with N-allyl-2,2,2-trifluoroacetamide following the method used in Example 10 except DMF was used as solvent gave (E)-N-(3-(3-(cyclohexylmethoxy)-5-fluorophenyl)allyl)-2,2,2-trifluoroacetamide as a white solid. Yield (0.44 g, 64%): 1H NMR (400 MHz, DMSO-d6) 1H NMR (400 MHz, CDCl3) δ 9.68 (t, J=4.0 Hz, 1H), 6.79-6.86 (m, 2H), 6.65 (dt, J=10.8, 2.0 Hz, 1H), 6.45 (d, J=15.6 Hz, 1H), 6.31 (dt, J=16.0, 5.6 Hz, 1H), 3.95 (t, J=4.8 Hz, 2H), 3.77 (d, J=5.6 Hz, 2H), 1.58-1.80 (m, 6H), 1.10-1.28 (m, 3H), 0.90-1.06 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982071B2
Source datasetuspto-grants-2011_07
ORD IDord-b7b896a913da4e008dee3c49b9817359
Source noteuspto-grants-2011_07