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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274529Generated: October 31, 2026

N-Methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamide → 1-[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]ethanone

https://huagongshe.com/reaction/2274529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamideHCID 87426929—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]ethanoneHCID 71650557—

Reaction Conditions

Temperature-78 °C

Reaction Steps

N-methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamide (7.5 g, 25.2 mmol) was dissolved in THF (84 mL) and cooled to −78° C. Methyl magnesium bromide (3N in diethyl ether, 21.03 mL, 63.1 mmol) was added dropwise and the resulting reaction mixture was stirred for 30 min. The reaction was warmed to 25° C. over 30 minutes and then was quenched by addition to an Erlenmeyer flask containing ice and saturated ammonium chloride solution. This mixture was extracted with EtOAc, the organic layers were collected and dried with anhydrous magnesium sulfate, then filtered and concentrated. Crude material obtained corresponds to 1-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]ethanone. 1H NMR (400 MHz, CDCl3) δ 2.62 (s, 3H), 5.96 (t, t, J=53, 2.7 Hz, 1H), 7.43 (d, J=8.1 Hz, 1H), 7.51 (t, J=8.0 Hz, 1H), 7.80 (s, 1H), 7.88 (d, J=7.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126976B2
Source datasetuspto-grants-2015_09
ORD IDord-075c418ed7ce4f118dd98dd015e5e640
Source noteuspto-grants-2015_09