HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → (S)-3-Hydroxy-4-morpholin-4-yl-4-oxo-butyric acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Acetoxy-4-morpholin-4-yl-4-oxo-butyric acid | HCID 22054036 | — |
| Reactant | (S)-3-Acetoxy-4-morpholin-4-yl-4-oxo-butyric acid | HCID 58619493 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-3-Hydroxy-4-morpholin-4-yl-4-oxo-butyric acid methyl ester | HCID 58619497 | — |
Reaction Steps
To a mixture of (S)-3-Acetoxy-4-morpholin-4-yl-4-oxo-butyric acid and 2-Acetoxy-4-morpholin-4-yl-4-oxo-butyric acid (11 g, 44.8 mmol) in dry methanol (30 mL) HCl in dioxane (4M, 7.3 ml, 29.16 mmol) was added and stirred at room temperature for 5 hrs. The reaction mixture was neutralized with solid NaHCO3, filtered through a mixture of Celite/Na2SO4 (1:1) and concentrated under reduced pressure. Column chromatography on silica eluting with a mixture of ethyl acetate and methylene chloride gave (S)-3-Hydroxy-4-morpholin-4-yl-4-oxo-butyric acid methyl ester (6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030116B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-85bb7806e90448aba9e1ebbf343ae9ee |
| Source note | uspto-grants-2006_04 |