HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 131733538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | HCID 86729623 | HCID 86729623 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131733538 | HCID 131733538 | — |
Reaction Steps
To a stirred solution of Intermediate 2 (1.9 g, 6.33 mmol) in dichloromethane:acetonitrile (700 mL), m-CPBA (1.19 g, 6.96 mmol) was added and stirred at rt for 1 h. TLC showed completion of starting material and formation of a polar spot (TLC System: 10% methanol/chloroform, (Rf): 0.4). The reaction mixture was concentrated, diluted with dichloromethane (30 ml), and washed with saturated sodium bicarbonate solution (20 mL) and water (15 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The crude compound was purified by silica gel column chromatography with 1 to 1.5% methanol in chloroform as eluents to afford Intermediate 3 as colorless gummy solid. (1.4 g, 70%). MS m/z: 317.1 (ES+, M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145387B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-bc227b52eeac403eabebb3fb93e91ebc |
| Source note | uspto-grants-2015_09 |