HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Bromo-o-fluorotoluene → HCID 71625272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Bromo-o-fluorotoluene | HCID 67968 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178445911 | HCID 178445911 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 71625272 | HCID 71625272 | 62.3% |
Reaction Steps
The product from step (a) (20 mg, 67 μmol) was suspended in dimethyl sulphoxide (450 μL) and Hunig's base (13 μL, 74 μmol) was added. 2-Fluorobenzyl bromide (8.0 μL, 67 μmol) was quickly added to the stirred solution. The reaction was stirred for 60 minutes to give a homogeneous solution The crude solution was diluted to 1 mL with acetonitrile and chromatographed on a reverse phase column using a gradient (40–70% acetonitrile) to give the title compound as a white solid (17 mg, 61% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067657B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-adeb0f851f6c4fb2bb34c5db435a003f |
| Source note | uspto-grants-2006_06 |