HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922314Generated: November 4, 2026
4-Hydroxybenzaldehyde → Benzaldehyde, 4-(phenylmethoxy)-
https://huagongshe.com/reaction/922314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | 64.75% |
Reaction Steps
To a 100 mL RB flask fitted with magnetic stirrer was charged 80 mL of acetonitrile. To the stirred solvent was added 4-hydroxy benzaldehyde (4 g, 33 mmol) and K2CO3 (9 g, 65 mmol). Then it was stirred for 5 min. Benzyl bromide (6.7 g, 39 mmol) was added. Then RM heated 80° C. for 2 h. After completion of the reaction (reaction monitored by TLC), the RM was concentrated in vacuum to remove the acetonitrile. To the residue was then added 100 mL of water and extracted with ethyl acetate (150 mL×2). The organic layer was washed with saturated brine solution (50 mL), dried over anhydrous Na2SO4 and evaporated to dryness gave the titled compound (4.5 g, 64.75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-765081428f1d47cfba15949ad7af0887 |
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| Source note | uspto-grants-2016_03 |
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