HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064908Generated: October 26, 2026
Sulfuric Acid → 1-Bromo-2-ethyl-4-[(phenylmethyl)oxy]benzene
https://huagongshe.com/reaction/1064908
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(Benzyloxy)-3-ethylbenzene | HCID 19744485 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Bromo-2-ethyl-4-[(phenylmethyl)oxy]benzene | HCID 15143471 | 83% |
Reaction Steps
To a solution of 1-ethyl-3-(phenylmethoxy)-benzene (15 g, 71 mmol) in THF (200 ml) were added N-bromosuccinimide (16.3 g, 92 mmol) and concentrated sulfuric acid (2.4 ml). The solution was stirred for 5 h at ambient temperature. Sodium bicarbonate (3.6 g) and 10% aqueous NaHSO3 solution (400 ml) were added under ice cooling. The resulting mixture was stirred for 10 min and then poured into ethyl acetate. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined extracts were washed with ice water and brine and dried over sodium sulfate. Removal of the solvent under reduced pressure gave a yellow oil which was purified by column chromatography (silica gel, cyclohexane) to yield 17.1 g (58.7 mmol, 83%) of the title compound as colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06969725B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-d448a34e780448448cc5a84ac8db2f88 |
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| Source note | uspto-grants-2005_11 |
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