HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702508Generated: October 29, 2026
Acetic Acid → 4-(Bromomethyl)-1-fluoro-2-phenoxybenzene
https://huagongshe.com/reaction/1702508
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 12922713 | HCID 12922713 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Bromomethyl)-1-fluoro-2-phenoxybenzene | HCID 12922714 | — |
Reaction Steps
A mixture of 14.7 g (0.05 mol) of 4-fluoro-3-phenoxy-benzyl phenyl ether, 50 ml of 32% strength aqueous hydrobromic acid and 60 ml of glacial acetic acid was heated to the reflux temperature for 10 hours, while stirring. The reaction mixture was then poured into 200 ml of water and extracted twice with 200 ml of methylene chloride each time. The combined methylene chloride phases were then extracted twice by shaking with 100 ml of 10% strength sodium hydroxide solution each time. The organic phase was subsequently dried over magnesium sulphate and the solvent was then stripped off under a waterpump vacuum. The residue was freed from the last residues of solvent by incipient distillation at a bath temperature of 60° C./3 mbars. 4-Fluoro-3-phenoxy-benzyl bromide was thus obtained as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04381412 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-e86101c5423b4540bd316bdaaac4a7f2 |
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| Source note | uspto-grants-1983_04 |
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