HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796133Generated: October 26, 2026
Acetonitrile → 2-(2-Methyl-propane-1-sulfonylmethyl)-4-morpholin-4-yl-4-oxo-butyric acid
https://huagongshe.com/reaction/1796133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Isobutyl-sulphinic acid | HCID 12672760 | — |
| Reactant | 2-Methylene4-morpholin-4-yl-4-oxo-butyric acid | HCID 22054022 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Methyl-propane-1-sulfonylmethyl)-4-morpholin-4-yl-4-oxo-butyric acid | HCID 11565984 | 28% |
Reaction Steps
A mixture of 2-Methylene-4-morpholin-4-yl-4-oxo-butyric acid (3.98 g, 20 mmol) and isobutyl-sulphinic acid (2.44 g, 20 mmol) were suspended in anhydrous toluene (80 mL) and anhydrous acetonitrile (20 mL). This mixture was warmed to 85° C. and stirred vigorously for 4.5 h. The reaction mixture was allowed to cool to room temperature and concentrated under vacuum. The residue was purified by flash chromatography using a 90 g silica gel column eluting with 10% methanol/CH2Cl2. Recovered 3.7 g of product as an oil. Triturated residue with isopropanol (5 mL)/ether (100 mL). Product began to precipitate out. Cooled this to 5° C. for 17 hrs(overnight). Product was collected by filtration, washed with ether and dried under vacuum to give 2-(2-Methyl-propane-1-sulfonylmethyl)-4-morpholin-4-yl-4-oxo-butyric acid as a white solid (1.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07030116B2 |
|---|
| Source dataset | uspto-grants-2006_04 |
|---|
| ORD ID | ord-01136e723d504499b19315b80684ec11 |
|---|
| Source note | uspto-grants-2006_04 |
|---|