HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 86750039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22447459 | HCID 22447459 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | DCM MeOH AcOH | HCID 21877243 | — |
| Product | HCID 86750039 | HCID 86750039 | — |
Reaction Steps
2-Nitrophenylglycine amide, 1 DMSO (500 mg, 1.83 mmol) was suspended in chloroform (20 ml) and triethylamine (390 μl, 2.80 mmol) was added. Subsequently benzoyl chloride (330 μl, 2.8 mmol) was added with stirring. The reaction was followed by TLC using as eluent: CH2Cl2 /MeOH/AcOH (85:10:5) and after 1 h at 20° C. the reaction mixture was treated with a saturated solution of NaHCO3, dried over anhydrous MgSO4 and evaporated to dryness. The product was recrystallized from absolute ethanol. Yield: 600 mg (77%); mp 178°-180° C., identified by 1H NMR spectroscopy. ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580751 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-741c454611c9440fb68c5158700b8fa1 |
| Source note | uspto-grants-1996_12 |