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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217756Generated: October 30, 2026

N-Methoxy-N-methyl-5-nitro-3-pentafluorosulfanylbenzamide → 3-Amino-N-methoxy-N-methyl-5-pentafluorosulfanylbenzamide

https://huagongshe.com/reaction/217756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methyl-5-nitro-3-pentafluorosulfanylbenzamideHCID 58136777—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product3-Amino-N-methoxy-N-methyl-5-pentafluorosulfanylbenzamideHCID 5808570345.2%

Reaction Steps

N-Methoxy-N-methyl-5-nitro-3-pentafluorosulfanylbenzamide (O6.075; 4.2 g) was dissolved in methanol (120 ml), and Raney nickel (about 700 mg) was added. With a hydrogen balloon attached, hydrogenation was effected on a magnetic stirrer. After 5 h, the catalyst was filtered off and washed with methanol. The filtrate was concentrated under reduced pressure and the residue was purified by means of preparative chromatography. The product-containing fractions were combined, freed of the acetonitrile, basified with sodium hydrogencarbonate solution and extracted three times with ethyl acetate. The combined extracts were dried over magnesium sulfate, filtered and concentrated. 1.73 g of the desired compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-c96d365ebaaf413caef24101c380d0f8
Source noteuspto-grants-2012_06