HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 23432059, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Hexen-1-ol | HCID 5318042 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 2-(4-Hydroxyphenyl)-5-pentylthiophene | HCID 23432314 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23432059 | HCID 23432059 | 15.2% |
Reaction Steps
Triphenylphosphine (0.53 g) was added in small portions to a solution of (E)-hex-2-en-1-ol (0.20 g), 2-(4-hydroxyphenyl)-5-pentylthiophene (0.50 g), diethylazodicarboxylate (0.35 g) in dry tetrahydrofuran (15 cm3) at 0° C. under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature overnight. The solvent was 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 0.10 g of 2-(4-[(E)-hex-2-enyloxy]phenyl)-5-pentylthiophene, K, 82° C., I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696110B1 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-b47bd7ec54a84912addb895eb428161a |
| Source note | uspto-grants-2004_02 |