HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397837Generated: October 30, 2026
Water → 1-[2-(Bromomethyl)phenoxy]-2,4-dichlorobenzene
https://huagongshe.com/reaction/397837
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | [2-(2,4-dichlorophenoxy)phenyl]methanol | HCID 2763668 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[2-(Bromomethyl)phenoxy]-2,4-dichlorobenzene | HCID 23001263 | 57.3% |
Reaction Steps
Phosphorus(III) tribromide (0.41 ml, 4.37 mmol) was added to a solution of 1-[2-(2,4-dichlorophenoxy)phenyl]methanol (420 mg, 1.56 mmol) in dioxane (10 ml). The reaction mixture was stirred for 1 hour at room temperature. Another portion of phosphorus(III) tribromide (0.41 ml, 4.37 mmol) was added. The reaction mixture was stirred for 16 hours at room temperature. It was cooled to 0° C. Water (5 ml) was added dropwise. The reaction mixture was warmed to room temperature and diluted with ethyl acetate (400 ml). It was washed with a 10% aqueous solution of sodium hydrogensulphate. The aqueous phase was extracted with ethyl acetate (50 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane 1:3 as eluent, to give 297 mg of 2-(2,4-dichlorophenoxy)benzyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610721B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-6908f7e111b5421792b182b6f382cb88 |
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| Source note | uspto-grants-2003_08 |
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