HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perfluorohexane → trans-Stilbene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perfluorohexane | HCID 9639 | — |
| Reactant | trans-beta-Bromostyrene | HCID 5314126 | — |
| Reactant | HCID 178506618 | HCID 178506618 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | trans-Stilbene | HCID 638088 | — |
| Product | trans-beta-Bromostyrene | HCID 5314126 | — |
Reaction Steps
FC-72 (10 mL) was charged to the U-tube (F-phase), a solution of (E)-bromostyrene (130 μL, 1.0 mmol) in MeCN (1 mL) was charged to the S-phase of the U-tube and a solution of Pd(PPh3)4 (23 mg, 0.02 mmol) in toluene (1.5 mL) was charged to the P-phase of the U-tube. After PhZnI (0.5 M in THF, 1.0 mL) was added to the P-phase, each phase was stirred for 1 day. The mixture in the P-phase was decanted into water, extracted with ether, dried over MgSO4 and then evaporated. However, trans-stilbene was not obtained in the P-phase and (E)-bromostyrene was recovered from the S-phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734318B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-4ee7cb7d88744415a0506a0300270c9b |
| Source note | uspto-grants-2004_05 |