HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483525Generated: October 26, 2026
Sodium amide → 1-{1-[4-(1-Butenyl)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril
https://huagongshe.com/reaction/483525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Propyltriphenylphosphonium bromide | HCID 80374 | — |
| Reactant | HCID 19030828 | HCID 19030828 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-{1-[4-(1-Butenyl)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril | HCID 53848495 | 931.7% |
Reaction Steps
To a mixture of propyltriphenylphosphonium bromide (2.34 g), potassium-t-butoxide (62 mg) and sodium amide powder (0.3 g) is added tetrahydrofuran (110 ml) under argon atmosphere and the mixture is stirred at room temperature for 3 hours. To the resulting yellowish red solution is added 1-[1-(4-formylbenzoyl)-4-piperidinyl]-3,4-dihydrocarbostyril (2 g) gradually under ice cooling and the mixture is stirred under the same conditions for 3 hours. The reaction mixture is poured into water and extracted with ethyl acetate/toluene and then dried over sodium carbonate. The resultant is purified by silica gel column chromatography (solvent: n-hexane:ethyl acetate=1:1) to give 1-{1-[4-(1-butenyl)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225402 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-3f1729f90cc54dfdb0d1a83b2428363f |
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| Source note | uspto-grants-1993_07 |
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