HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764932Generated: October 27, 2026
Triethylamine → 2-Bromo-5-fluoro-N-methoxy-N-methylbenzamide
https://huagongshe.com/reaction/1764932
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 2-Bromo-5-fluorobenzoic acid | HCID 2778181 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-5-fluoro-N-methoxy-N-methylbenzamide | HCID 22735479 | 73% |
Reaction Steps
2-Bromo-5-fluorobenzoic acid (4.60 g, 0.02 mol), N,O-Dimethylhydroxylamine hydrochloride (2.05 g, 0.02 mol), carbon tertabromide (6.9 g, 0.02 mol) was added to mixture of methylene chloride (100 mL) and triethylamine (2.9 mL, 0.02 mol). Triphenylphospine (5.53 g, 0.02 mol) was added to the solution over 1 hour and stirred for another 1 hour. The solution was concentrated to an oil. Hexanes (100 mL) and Ethyl Acetate (100 mL) were added to the oil and stirred for 1 hour then filtered. The filtrate was concentrated and the residue was purified by chromatography (Hexanes/Ethyl Acetate) on silica gel to afford 2-bromo-5-fluoro-N-methoxy-N-methylbenzamide as a foamy white solid in 73% yield. 1H NMR (CDCl3, 500 MHz) δ3.00-3.98 (m, 6 H), 6.97-7.08 (m, 2H), 7.51-7.54 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039679E1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-4e87e0b2dfe74e80acfec4a9a9307f5c |
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| Source note | uspto-grants-2007_06 |
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