HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-[(E)-hex-2-enyloxy]-5-(4'-hexylbiphenyl-4-yl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Hexen-1-ol | HCID 5318042 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 2-Hydroxy-5-(4'-hexylbiphenyl-4-yl)thiophene | HCID 23432173 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(E)-hex-2-enyloxy]-5-(4'-hexylbiphenyl-4-yl)thiophene | HCID 23432181 | 19.3% |
Reaction Steps
Triphenylphosphine (1.4 g) is added in small portions to a solution of (E)-hex-2-en-1-ol (0.60 g), 2-hydroxy-5-(4′-hexylbiphenyl-4-yl)thiophene (0.50 g), diethylazodicarboxylate (0.80 g) in dry tetrahydrofuran (100 cm3) at 0° C. under an atmosphere of nitrogen. The reaction mixture is stirred at room temperature overnight. The solvent is removed under reduced pressure and the crude product was purified by column chromatography on silica gel using a 4:1 petroleum (40-60° C.) ether/ethyl acetate mixture as eluent, followed by recrystallisation from ethanol to yield 0.12 g of 2-[(E)-hex-2-enyloxy]-5-(4′-hexylbiphenyl-4-yl)thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696110B1 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-31d202eed6e74b5e96675609941c9056 |
| Source note | uspto-grants-2004_02 |