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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458389Generated: November 4, 2026

Iodine → (4-Fluoro-3-phenoxyphenyl)-boronic acid

https://huagongshe.com/reaction/1458389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTrimethyl borateHCID 8470—
ReactantMagnesiumHCID 5462224—
ReactantBenzene, 4-bromo-1-fluoro-2-phenoxy-HCID 11076399—
Catalyst1,2-DibromoethaneHCID 7839—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(4-Fluoro-3-phenoxyphenyl)-boronic acidHCID 2118540482%

Reaction Steps

A solution of 5-bromo-2-fluorophenyl phenyl ether (8.01 g, 30 mmol) in tetrahydrofuran is added dropwise over 30 minutes to a mixture of magnesium turnings (0.0802 g, 33 mmol), a crystal of iodine and a few drops of 1,2-dibromoethane in tetrahydrofuran at 50°-55° C. under nitrogen. After the addition is complete, the reaction mixture is stirred at 50°-55° C. for 70 minutes and cooled to room temperature. The cooled mixture is added over 25 minutes to a solution of trimethyl borate (4.09 mL, 36 mmol) in diethyl ether at dry ice/acetone bath temperature. After the addition is complete, the mixture is stirred at dry ice/acetone bath temperature for 20 minutes, allowed to warm to -10° C. over 25 minutes, diluted sequentially with acetic acid and water, stirred at room temperature for 30 minutes, and extracted with ether. The organic extract is washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. A mixture of the residue in water is heated over a steam bath for 30 minutes, cooled to room temperature and filtered to obtain a solid which is washed with hexanes and dried to give the title product as a colorless solid (5.7 g, mp 177°-180° C., 82% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849958
Source datasetuspto-grants-1998_12
ORD IDord-1fd5000ff3d94deeac66493ba05b23d0
Source noteuspto-grants-1998_12