HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → HCID 10032156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 10347709 | HCID 10347709 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Diethylether water | HCID 21584184 | — |
| Product | HCID 10032156 | HCID 10032156 | 72% |
Reaction Steps
The compound of Example 26 (30 mg, 53.7 μmol) was added to 1.5 ml of nitromethane, 0.5 ml of THF, and 30 ml (0.25 mmol) benzyl bromide. The mixture was allowed to react at room temperature for 1 hour. The reaction mixture was poured into ethyl ether/water, and the ether layer was washed with brine, dried over sodium sulfate, and concentrated under vacuum. Flash chromatography of the residue on silica gel using 10:1 to 7:1 hexane/ethyl acetate (1% acetic acid) gave the product (25 mg, 38.5 μmol, 72% yield). High resolution mass spectrum, m/e 648.2490 (calculated for C36H42NO6S2 (M+H), 648.2453).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05192782 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-a3a8091cce0143969257982f23c2471e |
| Source note | uspto-grants-1993_03 |