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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606295Generated: October 25, 2026

Phosphoric Acid → (5-methyl-1H-indol-4-yl)boronic acid

https://huagongshe.com/reaction/606295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantTributyl borateHCID 12712—
ReactantPotassium hydrideHCID 82127—
Reactant4-bromo-5-methyl-1H-indoleHCID 10488635—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Product(5-methyl-1H-indol-4-yl)boronic acidHCID 5967815534.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 4-bromo-5-methylindole (800 mg, 3.8 mmol) in anhydrous ether (8 mL) is added with stirring to a suspension of potassium hydride (560 mg, 4.2 mmol, 30% dispersion in mineral oil) in anhydrous ether at 0° C. under argon. The resulting mixture is cooled to −78° C. and tert-butyllithium (4.9 mL of 1.7 M in pentane, 8.4 mmol) is slowly added. The resulting cream-colored mixture is stirred at −78° C. for 1 hour. Tributylborate (3.1 mL, 11.4 mmol) is slowly added and the reaction mixture is stirred for 1 hour at −78° C. before being allowed to slowly warm to room temperature. More anhydrous ether is added to facilitate stirring. After stirring for 24 hours, the resulting sticky mixture is diluted with ether and transferred in portions with stirring to a precooled solution of 1 M phosphoric acid (50 mL). After stirring for 30 minutes, the acidic mixture is extracted with diethyl ether (75 mL×3) and the combined extracts are extracted with 1 N sodium hydroxide (20 mL×4). The combined base extracts are cooled with an ice bath, acidified with 1 M phosphoric acid and extracted with ethyl acetate (20 mL×3). The combined extracts are washed with brine (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated to obtain a beige residue. The residue is triturated with hexane to obtain the desired 5-methylindole-4-boronic acid as a beige gum (230 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915288B2
Source datasetuspto-grants-2011_03
ORD IDord-10b3eec4ef0a4deba01a71182dc0c762
Source noteuspto-grants-2011_03