HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253231Generated: October 31, 2026
3-Phenoxybenzyl alcohol → 1-(Bromomethyl)-3-phenoxybenzene
https://huagongshe.com/reaction/1253231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Phenoxybenzyl alcohol | HCID 26295 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | 81.3% |
Reaction Steps
A solution of 3-phenoxybenzyl alcohol (36.0 grams, 0.18 mole) in toluene (95 ml) was added dropwise during a thirty minute period to a stirred solution of thionyl bromide (50 grams, 0.24 mole), pyridine (0.5 gram) and toluene (175 ml) while maintaining the temperature below 30° C. After the addition was complete,the reaction mixture was heated at 50°-60° C. for two hours. Upon cooling, the reaction mixture was concentrated under reduced pressure leaving a residue. This residue was dissolved in toluene (200 ml) and washed with water (10×100 ml) until a neutral pH was obtained. The dried (magnesium sulfate) toluene layer was concentrated under reduced pressure leaving a residue. This residue was distilled yielding 38.5 grams of 3-phenoxybenzyl bromide, b.p. 120°-144° C./0.05 mmHg. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04748186 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-69fb01d39f7f4424a92b50d176b82e6f |
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| Source note | uspto-grants-1988_05 |
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