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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantPyBOPHCID 2724699—
Reactant2-Fluoro-3-methoxybenzoic acidHCID 3390679—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-fluoro-N,3-dimethoxy-N-methylbenzamideHCID 1798192937%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410982B2
Source datasetuspto-grants-2008_08
ORD IDord-b698b4de439c490386a57658925ada89
Source noteuspto-grants-2008_08