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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172804Generated: October 30, 2026

N-Allyl-2,2,2-trifluoroacetamide → HCID 86635871, compound

https://huagongshe.com/reaction/2172804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Allyl-2,2,2-trifluoroacetamideHCID 558569—
Reactant3-bromo-N-cyclohexylbenzamideHCID 2306322—
ProductHCID 86635871HCID 86635871—

Reaction Steps

Heck coupling of 3-bromo-N-cyclohexylbenzamide and N-allyl-2,2,2-trifluoroacetamide following the method described in Example 118 gave (E)-N-cyclohexyl-3-(3-(2,2,2-trifluoroacetamido)prop-1-enyl)benzamide as a light yellow solid. Yield (0.50 g, 71%): 1H NMR (400 MHz, CD3OD) δ 8.18-8.26 (m, 1H), 7.83 (t, J=1.6 Hz, 1H), 7.65-7.68 (m, 1H), 7.54-7.56 (m, 1H), 7.39 (t, J=7.6 Hz, 1H), 6.62 (d, J=16.0 Hz, 1H), 6.32 (dt, J=16.0, 6.4 Hz, 1H), 4.06 (d, J=5.6 Hz, 2H), 3.80-3.90 (m, 1H), 1.93-1.95 (m, 2H), 1.79-1.82 (m, 2H), 1.66-1.70 (m, 1H), 1.18-1.48 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056849B2
Source datasetuspto-grants-2015_06
ORD IDord-d629803ff4f74c44a7360043adce7ad9
Source noteuspto-grants-2015_06