HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073869Generated: October 31, 2026
4-Hydroxybenzaldehyde → 4-(4-(2-Quinolinylmethyloxy)styryl)phenol
https://huagongshe.com/reaction/2073869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(2-Quinolinylmethyloxy)benzyl triphenylphosphonium chloride | HCID 19808942 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-(2-Quinolinylmethyloxy)styryl)phenol | HCID 53969192 | — |
Reaction Steps
A suspension of (13.29 mmol) of 4-(2-quinolinylmethyloxy)benzyl 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 (13.29 mmol) of 4-hydroxybenzaldehyde in 20 ml of DMF is dropped in over a period of 15 minutes. The reaction is allowed to equilibrate to 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)phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04920130 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-2fd738126b42402d808f97fd87fd276c |
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| Source note | uspto-grants-1990_04 |
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