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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249713Generated: October 25, 2026

Hydrochloric Acid → 1-(3-Dimethylamino-5-pentafluorosulfanylphenyl)ethanone

https://huagongshe.com/reaction/249713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant3-Dimethylamino-N-methoxy-N-methyl-5-pentafluorosulfanylbenzamideHCID 58085704—
ReactantHCID 178418573HCID 178418573—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(3-Dimethylamino-5-pentafluorosulfanylphenyl)ethanoneHCID 58085707—

Reaction Steps

3-Dimethylamino-N-methoxy-N-methyl-5-pentafluorosulfanylbenzamide (980 mg) was dissolved in abs. THF (50 ml) and methylmagnesium bromide solution (2.1 ml; 3 M solution in diethyl ether) was added dropwise at 0° C. with stirring. After addition was completed, the ice bath was removed and the mixture was stirred at RT for 1 h. To complete the reaction, more methylmagnesium bromide solution (0.3 ml) was added and the mixture was stirred for a further 2 h. After storage overnight in a refrigerator, the reaction mixture was treated with 1 N hydrochloric acid with cooling. After addition of water and ethyl acetate, it was extracted a further two times with ethyl acetate, and the combined organic phases were dried with magnesium sulfate, filtered and concentrated. The residue was purified by means of chromatography on silica gel (n-heptane/ethyl acetate 100/0 to 50/50 in 30 min). The product-containing fractions were combined, the solvent was removed and the residue was dried in a high vacuum. 650 mg of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863269B2
Source datasetuspto-grants-2011_01
ORD IDord-0f82f63cad6441638bdf37035af03afc
Source noteuspto-grants-2011_01