HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → HCID 21069658, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | Dimethyl [2,4,6-tri(propan-2-yl)phenyl]boronate | HCID 10934694 | — |
| Reactant | HCID 21069659 | HCID 21069659 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21069658 | HCID 21069658 | — |
Reaction Steps
2.0 g of 4,4′-dibromo-2,2′-diiodo-5,5′-dioctyloxy-1,1′-biphenyl synthesized as above was put in a 100 ml flask in an atmosphere of nitrogen and 20 ml of tetrahydrofuran was added to dissolve the same. Then, the tetrahydrofuran solution was cooled to −90° C. and 3.4 ml of 1.6M hexane solution was added dropwise. After 1-hour stirring, a solution of 1.5 g of magnesium bromide in 20 ml of tetrahydrofuran was added, warmed to room temperature, and stirred for 1 hour. The mixture was cooled again to −90° C., and 1.01 g of (2,4,6-triisopropylphenyl)dimethoxyborane was added. After warming, the mixture was allowed to react under reflux for 12 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157154B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-e46395004e664909bfd2812dc56a087b |
| Source note | uspto-grants-2007_01 |