HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → tert-Butyl 2-oxo-2-(thiophen-3-yl)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyl (2-(methoxy(methyl)amino)-2-oxoethyl)carbamate | HCID 4428209 | — |
| Reactant | HCID 178506590 | HCID 178506590 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 2-oxo-2-(thiophen-3-yl)ethylcarbamate | HCID 67995722 | 46% |
Reaction Steps
To a solution of the Weinreb amide 45 (1.53 g, 7 mmol) in anhydrous THF (10 mL) was added dropwise (over a 10-min period) a solution of thiophen-3-ylmagnesium iodide (0.3 M in THF, 50 mL) under nitrogen atmosphere at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 18 h. The mixture was poured into a saturated NH4Cl solution and extracted with EtOAc. The organic phase was dried over anhydrous MgSO4, filtered and evaporated under vacuum. The residue was further purified by silica column chromatography to provide the titled compound (776 mg, 46%). MNa+264.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586550B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-08bd0cdb854141ca9fb604c79b258954 |
| Source note | uspto-grants-2013_11 |