HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394695Generated: October 26, 2026
Benzyl Bromide → 1-(Benzyloxy)-3-ethylbenzene
https://huagongshe.com/reaction/1394695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Ethylphenol | HCID 12101 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Benzyloxy)-3-ethylbenzene | HCID 19744485 | 93% |
Reaction Steps
To a suspension of potassium carbonate (17 g, 123 mmol) in N,N-dimethylformamide (40 ml) was added a solution of 3-ethyl-phenol (14.8 ml, 123 mmol) in N,N-dimethylformamide (40 ml) at 2° C. under an argon atmosphere. After stirring for 50 min at 2° C., benzyl bromide (14.6 ml, 123 mmol) was added over a period of 15 min at 2° C. The suspension was stirred for additional 30 min at 2° C. and for 12 h at ambient temperature. After adding ice water (250 ml), the solution was extracted two times with diethyl ether. The combined extracts were washed two times with brine and dried over sodium sulfate. Evaporation of the solvent gave a yellow oil which was purified by column chromatography (silica gel, cyclohexane) to yield 24.3 g (114 mmol, 93%) of the title compound as yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348349B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-02918c1dd0a5465495a99a800767ed7d |
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| Source note | uspto-grants-2008_03 |
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