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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217783Generated: October 27, 2026

Tetrahydrofuran → 4'-Benzyloxy-2-bromopropiophenone

https://huagongshe.com/reaction/2217783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBromineHCID 24408—
Reactantp-BenzyloxypropiophenoneHCID 78246—
ReactantSodium BicarbonateHCID 516892—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4'-Benzyloxy-2-bromopropiophenoneHCID 10004097.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07408084B2
Source datasetuspto-grants-2008_08
ORD IDord-4402d61fa5964742a25301c169c815a9
Source noteuspto-grants-2008_08