HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438406Generated: November 3, 2026
2-Bromo-4-tert-butylbenzaldehyde → HCID 20382954, compound
https://huagongshe.com/reaction/1438406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-4-tert-butylbenzaldehyde | HCID 29923446 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20382954 | HCID 20382954 | 81.4% |
Reaction Steps
To a stirred suspension of methyltriphenylphosphonium bromide (12.3 g, 33.7 mmol) in anhydrous THF (40 ml) was added n-butyl lithium (1.60 mol/l, hexane solution) (33.7 mmol, 21.1 ml) at 0° C. After 30 minutes at 0° C., to this was added 2-bromo-4-tert-butylbenzaldehyde (4.06 g, 16.8 mmol)(prepared according to J. Med. Chem. 2005, 48, 71-90) in anhydrous THF (10 ml) at 0° C. The reaction mixture was stirred at ambient temperature for 3 hours. The mixture was quenched with saturated ammonium chloride solution and extracted with EtOAc. The combined solution was washed with brine, dried over sodium sulfate and concentrated in vacuo to give the crude product. The crude product was purified by column chromatography on silica gel, eluting with hexane, to afford the title compound (3.27 g, 81%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622589B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-07c7565ee8124b8db930fefbc750e56f |
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| Source note | uspto-grants-2009_11 |
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