HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029447Generated: October 30, 2026
4-Chlorobenzaldehyde → HCID 54040399, compound
https://huagongshe.com/reaction/1029447
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phosphine, triphenyl-, hydrobromide | HCID 517696 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 54040399 | HCID 54040399 | — |
Reaction Steps
To a suspension of 3-((2-methoxy)-2-propoxy)propyl)triphenyl phosphonium bromide (4.42 g, 10 mmoles) in THF (100 mL) was added n-BuLi (6 mL of 1.6M) at -78°. The reaction mixture was stirred at -78° for 30 min. 4-Chlorobenzaldehyde (1.4 g, 10 mM) was added and the reaction was warmed to RT. The reaction mixture was quenched with buffer and extracted with ethyl acetate. After evaporation of the ethyl acetate, the crude residue was dissolved in 25 mL THF and 5 mL of AcOH plus 5 mL H2O was added. The mixture was stirred for 2 hours at RT and evaporated. The residue was extracted with ethyl acetate, and the ethyl acetate evaporated. Flash chromatography of the residue using 25% ethyl acetate/hexane afforded the title compound as a mixture of cis and trans isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102881 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-4a6542f5319242d9937099d250830257 |
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| Source note | uspto-grants-1992_04 |
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