HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373944Generated: October 30, 2026
Sodium hydride → 4-(4-(2-Quinolinylmethyloxy)styryl)benzonitrile
https://huagongshe.com/reaction/373944
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4-Cyanobenzyl)triphenylphosphonium chloride | HCID 2724468 | — |
| Reactant | 4-(2-quinolinylmethoxy)Benzaldehyde | HCID 14578960 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-(2-Quinolinylmethyloxy)styryl)benzonitrile | HCID 54295323 | — |
Reaction Steps
A suspension of 5.51 g (13.29 mmol) of (4-cyanobenzyl)triphenylphosphonium chloride in 100 ml of dry DMF under positive nitrogen atmosphere is cooled to 0° C. and 0.50 g (20.77 mmol) of an 80% NaH in oil dispersion is added in small portions. The suspension is aged for 15 minutes at 0° C. followed by 45 minutes at room temperature to assure complete anion formation. The flask is cooled back to 0° C. and 3.5 g (13.29 mmol) of 4-(2-quinolinylmethyloxy)benzaldehyde in 20 ml of DMF is dropped in over a period of 15 minutes. The reaction is allowed to equilibrate at room temperature and stirred for 2 hours. The resultant mixture is poured into ice water and filtered. The precipitate is dissolved in CH2Cl2, dried, and concentrated in vacuo. The crude product is recrystallized from ether to give 4-(4-(2-quinolinylmethyloxy)styryl)benzonitrile. (M.P. 116° C.-112° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166210 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-24858aff933b4c45bc2f0007464e9d9e |
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| Source note | uspto-grants-1992_11 |
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