HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292218Generated: November 1, 2026
HCID 21277002, compound → HCID 21277005, compound
https://huagongshe.com/reaction/2292218
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21277002 | HCID 21277002 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21277005 | HCID 21277005 | — |
Reaction Steps
To a suspension of 0.56 g of methyltriphenylphosphonium bromide in 10 ml of dry tetrahydrofuran were added 0.88 ml of a 1.6 molar n-butyllithium solution in hexane. After stirring for 3 hours under a nitrogen atmosphere, 0.5 g of 5-[3-methoxy-4-(2-methoxybenzoyl)-2-propylphenoxy]pentanenitrile were added in 5 ml of tetrahydrofuran. The reaction was stirred for 40 hours at 25° C. and then at 65° C. for 24 hours. After cooling to room temperature, the reaction mixture was filtered and the filtrate was evaporated to dryness. The residue was purified by preparative thin layer chromatography using a solvent system of 10% ethyl acetate in hexane. The appropriate band was isolated, extracted with ethyl acetate, dried over sodium sulfate, and evaporated in vacuo providing 50 mg of the desired title product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801616 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-3e41952426a9497eb04c465b27c2548f |
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| Source note | uspto-grants-1989_01 |
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