HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958797Generated: November 3, 2026
Benzyl Bromide → 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde
https://huagongshe.com/reaction/1958797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Ethyl-4-hydroxy-5-methylbenzaldehyde | HCID 23159210 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde | HCID 86639348 | 83.1% |
Reaction Steps
To a solution of 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (34.9 g, 0.213 mol) in MeCN (350 mL), K2CO3 (58.7 g, 0.425 mol) and benzylbromide (36.4 g, 0.213 mol) is added. The mixture is stirred at 60° C. for 2 h before it is cooled to rt, diluted with water and extracted twice with EA. The org. extracts are washed with water and concentrated to give crude 4-benzyloxy-3-ethyl-5-methyl-benzaldehyde as an orange oil (45 g). 1H NMR (CDCl3): δ1.29 (t, J=7.5 Hz, 3H), 2.40 (s, 3H), 2.77 (q, J=7.8 Hz, 2H), 4.90 (s, 2H), 7.31-7.52 (m, 5H), 7.62 (d, J=1.5 Hz, 1H), 7.66 (d, J=1.8 Hz, 1H), 9.94 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410151B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-dcada21f880745a78ba3c16194d3e0ab |
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| Source note | uspto-grants-2013_04 |
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