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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657983Generated: October 29, 2026

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

https://huagongshe.com/reaction/657983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantMethyl 3-methoxy-5-(pentafluorosulfanyl)benzoateHCID 58136953—
ReactantHCID 178418365HCID 178418365—
SolventTetrahydrofuranHCID 8028—
Product3,N-Dimethoxy-N-methyl-5-(pentafluorosulfanyl)benzamideHCID 5813696864.8%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Methyl 3-methoxy-5-(pentafluorosulfanyl)benzoate (O4.007; 2.5 g) was dissolved in absolute THF (65 ml), and N,O-dimethylhydroxylamine hydrochloride (1.2 g) was added. Then the mixture was cooled to −15° C. and isopropylmagnesium bromide solution (13.59 ml, 2 M in THF) was added dropwise. After 20 min, the cooling bath was removed and the mixture was stirred at RT for 1 h. Then ammonium chloride solution was added and the aqueous phase was extracted three times with ethyl acetate. The combined extracts were dried over magnesium sulfate, filtered and concentrated. The crude product thus obtained still contained significant reactant, and was therefore converted and worked up again as described above. No reactant was present any longer in the residue which was then obtained. Purification was effected by means of preparative HPLC (met. A). The product-containing fractions were combined and freed of the acetonitrile, and the aqueous phase was extracted three times with EA. The combined extracts were dried over magnesium sulfate, filtered and concentrated. 1.78 g of the desired compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076336B2
Source datasetuspto-grants-2011_12
ORD IDord-058e8ca8eb854d3c9f583e52149a51c1
Source noteuspto-grants-2011_12