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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258524Generated: November 2, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → 3-Bromo-N-methoxy-N-methyl-5-(pentafluorosulfanyl)benzamide

https://huagongshe.com/reaction/1258524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58137421HCID 58137421—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
Product3-Bromo-N-methoxy-N-methyl-5-(pentafluorosulfanyl)benzamideHCID 5813746476.1%

Reaction Steps

3-Bromo-5-(pentafluorosulfanyl)benzoic acid (1.35 g) was dissolved in thionyl chloride (10 ml) while stirring, and kept under reflux with exclusion of moisture for 5 h. Then the thionyl chloride was drawn off, the residue was taken up in DCM (40 ml) and the solution was admixed with N,O-dimethylhydroxylamine hydrochloride (381 mg). Subsequently Hünig's base (0.7 ml) was added and then the mixture was stirred for 2 h. Thereafter, the mixture was dried, the residue was taken up with EA and the solution was washed five times with water. The EA phase was dried over magnesium sulfate, filtered and concentrated. The residue was purified using silica gel (60 g cartridge, 4:1 n-heptane/EA). 1.1 g of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466169B2
Source datasetuspto-grants-2013_06
ORD IDord-9da0dae061a34660bdf2b7b8c442838a
Source noteuspto-grants-2013_06