HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 53952497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(Benzyloxy)-5-bromobenzaldehyde | HCID 733087 | — |
| Reactant | Benzyltriphenylphosphonium bromide | HCID 2734970 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53952497 | HCID 53952497 | 88% |
Reaction Steps
To a stirred suspension of benzyl triphenylphosphonium bromide (7.44 g, 17.2 mmol) in freshly distilled THF (60 ml), under argon, was added a solution of LiN(SiMe3)2 (18.2 ml, 1N). The resulting red solution was allowed to stir for 30 minutes, then a solution of 5-bromo-2-benzyloxybenzaldehyde (5.0 g, 17.2 mmol) in freshly distilled THF (15 ml) added. The reaction was stirred at ambient temperature for 60 hours, treated with 1N aqueous HCl (60 ml) and extracted with ethyl ether (2×). The combined etherial extracts were washed with brine, dried (MgSO4) and evaporated. The residue was purified by chromatography (eluant:hexane) to give β-(2-benzyloxy-5-bromophenyl)styrene as a white solid (5.5 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965741 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-3f600bb2a86347b3a928ca0d57ac78e8 |
| Source note | uspto-grants-1999_10 |