HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394141Generated: November 1, 2026
Pyridine → 1-(Bromomethyl)-2,4-dimethoxybenzene
https://huagongshe.com/reaction/2394141
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 2,4-Dimethoxybenzyl alcohol | HCID 81750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Bromomethyl)-2,4-dimethoxybenzene | HCID 15151907 | — |
Reaction Steps
2 g (11.77 mmol) of 2,4-dimethoxybenzyl alcohol (Aldrich, Steinheim, FRG) are dissolved in 30 ml of abs. toluene, and this solution is treated with 0.3 ml of pyridine. The clear solution is cooled down to approximately 4° C. and 1.12 ml (0.992 equivalents) of PBr3 in 6 ml of abs. toluene are added dropwise to it over the space of 30 min. After a further 45 min, the reaction solution is poured onto ice-water and the whole is extracted with ether. The organic phase is washed, in succession, with water, sat. sodium bicarbonate solution and saline (all being cold). The combined aqueous phases are reextracted with ether. The combined organic phases are dried over Na2SO4 and the ether is removed on a RE at about 30° C. The toluene solution which remains, and which contains the title compound, is immediately subjected to further use. TLC (hexane:ethyl acetate, 1:1): decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807891 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-5af4e35de4404e17a73bdc777a9e1cd4 |
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| Source note | uspto-grants-1998_09 |
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