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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217785Generated: November 3, 2026

Tetrahydrofuran → 2-Bromo-1-phenylbutan-1-one

https://huagongshe.com/reaction/2217785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantButyrophenoneHCID 10315—
ReactantBromineHCID 24408—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-1-phenylbutan-1-oneHCID 52696—

Reaction Steps

To a tetrahydrofuran solution (20 mL) of 9.917 g (67.0 mmol) of butyrophenone, a hexane solution (10 mL) of 11.78 g (1.1 equivalents) of bromine was gradually added at 5° C. The temperature was elevated to 15° C., and the solution was stirred for 1 hour. To the solution, 20 mL of water and 40 mL of ethyl acetate were added to conduct extraction. The organic layer was washed with 30 mL of a saturated sodium hydrogen carbonate solution three times, dried over anhydrous magnesium sulfate, and subjected to distillation under a reduced pressure to remove the solvents. 1-Phenyl-2-bromo-1-butanone was obtained as a light peach-colored oily substance (23.94 g, crude yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07408084B2
Source datasetuspto-grants-2008_08
ORD IDord-27c45f464afc43e0b416843672e60113
Source noteuspto-grants-2008_08