HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl glycidyl ether → HCID 71254084, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl glycidyl ether | HCID 31217 | — |
| Reactant | HCID 21107343 | HCID 21107343 | — |
| Reactant | HCID 71253927 | HCID 71253927 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71254084 | HCID 71254084 | — |
| Product | HCID 71254239 | HCID 71254239 | — |
Reaction Steps
MeLi (1.6 M in Et2O, 108 μl, 0.17 mmol) was added to a solution of the mixture of 6-bromo-9H-carbazole-3-carbonitrile and 9H-carbazole-3-carbonitrile (24.1 mg) in THF (1.0 mL) at −78° C. and stirred for 40 min. Phenyl glycidyl ether (24.1 mg, 0.16 mmol) was added at −78° C. and the reaction was stirred at 45° C. overnight. Upon completion, the solution was quenched with H2O. Ethyl acetate was added and the mixture was washed with H2O, and saturated aqueous NaCl. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. A small fraction was purified by reverse HPLC to afford the title products P7C3-S154 and P7C3-S155.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877797B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-7b87678618c64670b4537bf056bfb57a |
| Source note | uspto-grants-2014_11 |