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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424800Generated: October 26, 2026

4-Iodo-3-methylbenzoic acid → (4-Iodo-3-methylphenyl)methanol

https://huagongshe.com/reaction/424800

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-3-methylbenzoic acidHCID 1517322—
SolventTetrahydrofuranHCID 8028—
Product(4-Iodo-3-methylphenyl)methanolHCID 5384360195%

Reaction Steps

To a solution of 4-iodo-3-methyl-benzoic acid (5.2 g, 20 mmol) in THF (30 mL), is added 2.0 M borane-dimethyl sulfide complex in THF (40.0 mL, 80 mmol) dropwise. The reaction mixture is stirred overnight. The reaction mixture is quenched carefully at 0° C. with methanol (20 mL) and the mixture is evaporated to dryness under reduced pressure. The residue is partitioned between EtOAc (80 mL) and water (60 mL). The organic phase is washed with brine (60 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography (AnaLogix, gradient EtOAc/Hexane) to give (4-Iodo-3-methyl-phenyl)-methanol as white solid (4.7 g, 95%). 1HNMR (CDCl3) (ppm): 2.4 (3H, s), 4.55 (2H, s), 6.8-7.75 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106077B2
Source datasetuspto-grants-2012_01
ORD IDord-c972eae0d6c14fa291d1d2d6dbb11997
Source noteuspto-grants-2012_01