HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218092Generated: October 27, 2026
Triethylamine → 2-fluoro-N,3-dimethoxy-N-methylbenzamide
https://huagongshe.com/reaction/2218092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 2-Fluoro-3-methoxybenzoic acid | HCID 3390679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-fluoro-N,3-dimethoxy-N-methylbenzamide | HCID 17981929 | 37% |
Reaction Steps
To a solution of 2-fluoro-3-methoxy-benzoic acid (5.0 g, 29.4 mmol) and PyBOP (13.7 g, 29.4 mmol) in 7:1 CH2Cl2:THF was added triethylamine (4.10 mL, 29.4 mmol) over a 10 min period. N,O-Dimethylhydroxylamine hydrochloride (2.87 g, 29.4 mL) was then added and the reaction was allowed to stir at rt for 3 h. The reaction was then partitioned between dichloromethane and water. The organic phase was separated and the aqueous phase was extracted with 2×100 mL dichloromethane. The combined organic phases were dried (MgSO4) and concentrated in vacuo. The residue was taken up in ethyl acetate and was washed successively with 1N HCl, saturated aqueous NaHCO3, and brine. The organic phase was again dried (MgSO4) and concentrated in vacuo to yield the title compound (2.30 g, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410982B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-b698b4de439c490386a57658925ada89 |
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| Source note | uspto-grants-2008_08 |
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