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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234383Generated: October 25, 2026

Iodine → (4-Propylphenyl)boronic acid

https://huagongshe.com/reaction/234383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTrimethyl borateHCID 8470—
Reactant(3-Bromopropyl)benzeneHCID 12503—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(4-Propylphenyl)boronic acidHCID 4100861—

Reaction Steps

To a suspension of magnesium shavings (21 7 mg, 8.9 mmol) in 3 mL of dry tetrahydrofuran under argon, a crystal of iodine along with a solution of 4-bromopropylbenzene (1.69 g, 8.5 mmol) dissolved in 6 mL of tetrahydrofuran was added at such a rate that a gentle reflux was maintained. The solution was refluxed for an additional 0.5 h, cooled to room temperature and added in portions over 10 min to a solution of trimethylborate (924 mg, 8.9 mmol) previously dissolved in 4 mL of dry ether at -78° C. After 30 minutes, the solution was warmed to room temperature; and stirring was continued for 90 min. The reaction was then quenched by the addition of 2 mL of a 10% hydrochloric acid solution. The tetrahydrofuran was removed under reduced pressure and the remaining residue was extracted into diethyl ether (3×25 mL). The combined ether extracts was extracted with 1M NaOH (3×25 mL) and the resulting aqueous layer was acidified to pH 2.0 using 6N HCl, then reextracted back into diethyl ether (3×25 mL). The combined organic layers was washed with water (1×25 mL), brine (1×25 mL) and dried over magnesium sulfate. Evaporation of solvent left a brown solid which was filtered through a small plug of silica gel using 10% MeOH/CHCl3. Evaporation left 448 mg (32%) of a brown solid, m.p. 90°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-77ffbb9eb6944354beed97e5ef986ca4
Source noteuspto-grants-1997_01