HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 22941145, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 86753519 | HCID 86753519 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22941145 | HCID 22941145 | — |
Reaction Steps
Trimethylsulfoxonium iodide (9.9 g, 45 mmol) was added in small portions to a suspension of sodium hydride (1.8 g, 45 mmol) in DMF (120 mL). After the foaming had subsided (10 min), a solution of (trans)-N-methoxy-N-methyl-3-(2,3-dihydrobenzofuran-4-yl)propenamide (3.5 g, 15 mmol) in DMF (60 mL) was added dropwise, with the temperature maintained between 35°-40° C. The mixture was stirred for 3 h at room temperature. Saturated NH4Cl (50 mL) was added dropwise and the mixture was extracted three times with ethyl acetate. The organic extracts were combined, washed with H2O and brine, dried over K2CO3, and concentrated in vacuo to give a white wax (3.7 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856529 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-77b1151bad6a435bbbfa1a78a47c33f4 |
| Source note | uspto-grants-1999_01 |