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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240299Generated: October 29, 2026

Iodine → Hydroxy-phenyl-o-tolyl-acetic acid

https://huagongshe.com/reaction/2240299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-BromotolueneHCID 7236—
ReactantPhenylglyoxylic AcidHCID 11915—
ReactantSodium hydrideHCID 24758—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHydroxy-phenyl-o-tolyl-acetic acidHCID 226676—

Reaction Steps

To a stirred suspension of magnesium (0.773 g, 31.81 mmol), iodine (cat. Amount) in THF (20 ml) is added dropwise, bromotoluene (3.83 ml, 31.81 mmol) in THF (30 ml). The reaction mixture is warmed to initiate the reaction and then allowed to stir at room temperature for 30 minutes. Meanwhile, a second mixture comprising benzoyl formic acid (4.342 g, 28.92 mmol) in THF (50 ml) is cooled in an ice bath. Sodium hydride (1.156 g of a 60% dispersion in mineral oil, 28.92 mmol) is added to the mixture, portionwise, ensuring the temperature does not rise above 10° C. Then the grignard reagent which has been stirring for 30 minutes is added dropwise and the reaction mixture is allowed to warm to room temperature. After stirring for 21 hours, the reaction mixture is partitioned between ethyl acetate (150 ml) and water (150 ml). The aqueous layer is acidified to pH 1 with 1 M hydrochloric acid and then extracted with ethyl acetate. The organic portions are combined, washed with brine, dried over MgSO4 and concentrated in vacuo. The crude residue is purified by chromatography on silica (eluting with ethyl acetate) to yield the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723356B2
Source datasetuspto-grants-2010_05
ORD IDord-c7b404945abf414ab5ee5825f0dd5a55
Source noteuspto-grants-2010_05