HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398116Generated: October 27, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-Bromo-2-fluoro-N-methoxy-N-methylbenzamide
https://huagongshe.com/reaction/1398116
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-2-fluorobenzoic acid | HCID 302681 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,O-dimethoxyhydroxylamine hydrochloride | HCID 22015712 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-2-fluoro-N-methoxy-N-methylbenzamide | HCID 53211063 | 121.2% |
Reaction Steps
To a mixture of 4-bromo-2-fluorobenzoic acid (10 g) in DMF (4.0 mL) were added N,O-dimethoxyhydroxylamine monohydrochloride (5.3 g), HOBt (8.0 g), N-ethyldiisopropylamine (23 mL) and WSC (11 g), and the mixture was stirred at room temperature for 9 hr, and then at 40° C. for 38 hr. The reaction mixture was allowed to cool to room temperature, saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with 1N aqueous sodium hydroxide solution, water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (13 g). 1H NMR (300 MHz, CDCl3) δ 3.35 (3H, s), 3.55 (3H, brs), 7.29-7.40 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901309B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-4ba80ddf4f8649f9985788218e356758 |
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| Source note | uspto-grants-2014_12 |
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