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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methoxy-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)benzamide | HCID 87426929 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]ethanone | HCID 71650557 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126976B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-075c418ed7ce4f118dd98dd015e5e640 |
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| Source note | uspto-grants-2015_09 |
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