HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217783Generated: October 27, 2026
Tetrahydrofuran → 4'-Benzyloxy-2-bromopropiophenone
https://huagongshe.com/reaction/2217783
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | p-Benzyloxypropiophenone | HCID 78246 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-Benzyloxy-2-bromopropiophenone | HCID 100040 | 97.5% |
Reaction Steps
To 100 mL of a tetrahydrofuran solution of 24.00 g (100 mmol) of 4-benzyloxypropiophenone, a hexane solution (20 mL) of 23.973 g (1.5 equivalents) of bromine was gradually added at 20° C., followed by 1 hour of stirring. To the resulting solution, 50 mL of a saturated sodium hydrogen carbonate solution and 100 mL of ethyl acetate were added to conduct extraction. The organic layer was washed with 30 mL of a 20 wt % sodium thiosulfate aqueous solution, dried over anhydrous magnesium sulfate, and subjected to distillation under a reduced pressure to remove the solvents. A colorless, oily substance was obtained as a result. To this substance, 200 mL of hexane was added to precipitate crystals. White crystals (31.12 g; isolation yield: 95%) of 1-[4-(benzyloxy)phenyl]-2-bromo-1-propanone were obtained as a result.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07408084B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-4402d61fa5964742a25301c169c815a9 |
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| Source note | uspto-grants-2008_08 |
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