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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274528Generated: October 31, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → N-Methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamide

https://huagongshe.com/reaction/2274528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant3-(1,1,2,2-Tetrafluoroethoxy)benzoic acidHCID 578680—
SolventDimethylformamideHCID 6228—
ProductN-Methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamideHCID 87426929—

Reaction Conditions

Temperature25 °C

Reaction Steps

3-(1,1,2,2-tetrafluoroethoxy)benzoic acid (10 g, 42.0 mmol) was dissolved in DMF (200 mL) and Hunig's Base (20.54 mL, 118 mmol). Benzotriazol-1-yl-oxy-tris-(dimethylamino)phosphonium hexafluorophosphate (BOP, 27.9 g, 63.0 mmol) and N-methoxy-N-methylamine hydrochloride (4.51 g, 46.2 mmol) were added to the reaction flask, and the resulting reaction mixture was stirred at 25° C. overnight. Crude reaction mixture was concentrated and purified on a silica gel column (340 g cartridge 0-10% EtOAc/Hexanes gradient) to afford N-methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamide. 1H NMR (400 MHz, CDCl3) δ 3.38 (s, 3H), 3.57 (s, 3H), 5.95 (t, J=52.9, 2.9 Hz, 1H), 7.33 (d, J=8.1 Hz, 1H), 7.45 (t, J=7.9 Hz, 1H), 7.58 (s, 1H), 7.63 (d, J=7.7 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126976B2
Source datasetuspto-grants-2015_09
ORD IDord-b7ad90db5aff472b8a2847876db54a1f
Source noteuspto-grants-2015_09