HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989823Generated: November 2, 2026
HCID 11369822, compound → HCID 11243225, compound
https://huagongshe.com/reaction/1989823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11369822 | HCID 11369822 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11243225 | HCID 11243225 | — |
Reaction Steps
A suspension of methyltriphenylphosphonium bromide (11.4 g, 0.032 mol) in dry THF (100 mL) was cooled to 0° C. under argon. n-BuLi (2.5M, 12 mL, 0.030 mol) was added slowly. The suspension became more homogenous. The resulting clear orange solution of the ylide was stirred for another 15 min at 0° C. 2-(5-Bromo-2-chloro-4-methoxy-phenyl)-2-methyl-propionaldehyde (7.8 g, 0.027 mol) was dissolved in dry THF (50 mL) and added to ylide-solution. The mixture was stirred for 3 h/25° C. and the resulting suspension was quenched with MeOH (10 mL). The solvent was removed under reduced pressure and the crude product was purified by flash chromatography using n-heptane as eluent. Yield: 3.92 g (50%). GCMS: >99%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642367B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-927cb8bdb22340b694c0138a24b810a7 |
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| Source note | uspto-grants-2010_01 |
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