HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043425Generated: October 31, 2026
4'-Bromo-5-chlorobiphenyl-2-carbaldehyde → 4'-Bromo-5-chloro-2-vinylbiphenyl
https://huagongshe.com/reaction/1043425
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-Bromo-5-chlorobiphenyl-2-carbaldehyde | HCID 59266542 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Bromo-5-chloro-2-vinylbiphenyl | HCID 59266522 | 83% |
Reaction Steps
BuLi (2.5M in hexanes, 11.3 mL, 28.2 mmol) was added to a solution of methyltriphenylphosphonium bromide (10.1 g, 28.2 mmol) in THF (65 mL). The mixture was stirred at 0° C. for 1 hr. A solution of 4′-bromo-5-chlorobiphenyl-2-carbaldehyde (4.2 g, 14.11 mmol) in THF (65 mL) was added dropwise at 0° C. The mixture was stirred overnight from 0° C. to r.t. The reaction was filtered and evaporated. The residue was diluted with diethyl ether and washed with water and brine. The ether layer was collected, dried (MgSO4), filtered and evaporated to give the crude material. The crude material was purified on the Biotage (5-15% EtOAc:Hex) to give 4′-bromo-5-chloro-2-vinylbiphenyl (3.43 g, 11.68 mmol, 83% yield) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563505B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7d1c35633e104719b67a550b1e578ede |
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| Source note | uspto-grants-2013_10 |
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