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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Dimethylamino-N-methoxy-N-methyl-5-pentafluorosulfanylbenzamide | HCID 58085704 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3-Dimethylamino-5-pentafluorosulfanylphenyl)ethanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07863269B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-0f82f63cad6441638bdf37035af03afc |
|---|
| Source note | uspto-grants-2011_01 |
|---|