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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909087Generated: October 27, 2026

4-Bromophenol → 2-[(4-Bromophenoxy)methyl]-2-methyloxirane

https://huagongshe.com/reaction/1909087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)-2-methyloxiraneHCID 95220—
Product2-[(4-Bromophenoxy)methyl]-2-methyloxiraneHCID 66336120—

Reaction Steps

4-Bromophenol (80 g, 462 mmol), 2-(chloromethyl)-2-methyloxirane (400 ml) and potassium carbonate (95.86 g, 693 mmol) were mixed and allowed to react at 100° C. for 4 hours. After the reaction was completed, the mixture was concentrated under reduced pressure. Ethyl acetate (200 ml) and water (400 ml) were added thereto, followed by extraction. The water layer was extracted with ethyl acetate (200 ml). The organic layer was washed with water (200 ml) twice. The organic layer was then concentrated under reduced pressure to remove the ethyl acetate. Thereafter, toluene was added and the resulting mixture was concentrated under reduced pressure, obtaining 120 g of crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598358B2
Source datasetuspto-grants-2013_12
ORD IDord-023e6a7af9ab4b9580fc9acc9b99ab86
Source noteuspto-grants-2013_12