HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[N-(2,4,6-Trifluorophenyl)sulfamoyl]-acetic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide] → 2-[N-(2,4,6-trifluorophenyl)sulfamoyl]-acetic acid-[2,3,4-trihydroxy-butylamide]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[N-(2,4,6-Trifluorophenyl)sulfamoyl]-acetic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide] | HCID 15057603 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[N-(2,4,6-trifluorophenyl)sulfamoyl]-acetic acid-[2,3,4-trihydroxy-butylamide] | HCID 67825267 | — |
Reaction Steps
2.22 g (6 mmol) of 2-[N-(2,4,6-trifluorophenyl)sulfamoyl]-acetic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethyl-amide] is dissolved in a mixture of 10 ml of methanol and 5 ml of water, about 100 mg of cation exchanger Amberlyst 15 is added and it is warmed to boiling temperature in 1 hour. The ion exchanger is then filtered off and the filtrate is evaporated to dryness in a vacuum. 1.94 g (5.24 mmol) =87.3% of the theoretical yield of the product is obtained as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130119 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-3f4c72f5eaa4483c855695dcbf2ca698 |
| Source note | uspto-grants-1992_07 |