HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Methanesulfonyl-furan-2-carboxylic acid methoxy-methyl-amide → 1-(5-Methanesulfonyl-furan-2-yl)-propan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Methanesulfonyl-furan-2-carboxylic acid methoxy-methyl-amide | HCID 59278485 | — |
| Reactant | HCID 178461633 | HCID 178461633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Methanesulfonyl-furan-2-yl)-propan-1-one | HCID 59278141 | — |
Reaction Steps
To a chilled (0° C.) solution of 5-methanesulfonyl-furan-2-carboxylic acid methoxy-methyl-amide (1.48 g, 6.36 mmol) in THF (30 mL) was added a 2 M solution of ethylmagnesium chloride in THF (7.0 mL, 14 mmol). The mixture was then slowly warmed to with stifling. After 18 hours, the mixture was quenched with saturated aqueous ammonium chloride (50 mL) and then diluted with ethyl acetate (50 mL). The aqueous phase was separated and extracted with ethyl acetate (3×30 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated to afford 1-(5-methanesulfonyl-furan-2-yl)-propan-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063065B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-b2073fade71b4f3b82eda67b80d7bdbc |
| Source note | uspto-grants-2011_11 |