HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739404Generated: October 30, 2026
4-Hydroxybenzaldehyde → 4-(2-Phenoxyethoxy)benzaldehyde
https://huagongshe.com/reaction/1739404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21841067 | HCID 21841067 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Phenoxyethoxy)benzaldehyde | HCID 13483216 | 64.4% |
Reaction Steps
1.19 g of 4-hydroxybenzaldehyde were dissolved in 30 ml of DMF, and 0.41 g of 60% NaH were further added to the resultant solution while cooling it with ice. The solution was then stirred for 1 hour after elevating the temperature of the solution up to room temperature. The solution was again cooled with ice, then added with 2.0 g of 2-phenoxyethyl-methane sulfonate, and stirred for 1 hour at room temperature and subsequently for a night at 50-60° C. The solution reacted was poured into ice-water and extracted with ethyl acetate, then the organic layer resulted was dried with anhydrous magnesium sulfate. The solvent used was then removed by distillation under reduced pressure, and the residue obtained was washed with a mixture of ether and hexane, thereby affording 1.45 g of 4-(2-phenoxyethyloxy)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965743 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-2070c0609afe47438e3a39baf707cd68 |
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| Source note | uspto-grants-1999_10 |
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