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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426733Generated: November 1, 2026

Bromide ion → HCID 21105423, compound

https://huagongshe.com/reaction/2426733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantDisodium disulfiteHCID 24346—
ReactantBromineHCID 24408—
ReactantHCID 21105303HCID 21105303—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21105423HCID 21105423—

Reaction Steps

A solution of 0.449 g of 1-[3-fluoro-4-(1-methylbutoxy)phenyl]ethanone in 6.8 ml of dioxane was dropped dropwise into 1.36 g of NaOH, 1.6 g of bromine in 6.8 ml of water. The mixture was stirred at room temperature for 30 minutes and then heated at 50° C. for 1 h. The excess bromide was decomposed by adding a sodium disulfite solution, and then the solution was poured into 25% strength hydrochloric acid solution and stirred for 20 minutes. The solution was extracted with ethyl acetate. The combined organic phases dried over sodium sulfate, concentrated in vacuo and purified by preparative HPLC. This resulted in the product with the molecular weight of 226.1 (C12H15FO3); MS (ESI): 227 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968550B2
Source datasetuspto-grants-2011_06
ORD IDord-6211f177653f425e86645b67d5dd3f6e
Source noteuspto-grants-2011_06