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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383341Generated: October 31, 2026

Methanol → HCID 67308872, compound

https://huagongshe.com/reaction/2383341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium potassium tartrate tetrahydrateHCID 2724148—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 67309633HCID 67309633—
SolventDichloromethaneHCID 6344—
ProductHCID 67308872HCID 6730887270.6%

Reaction Steps

To a solution of 5-fluoro-2-iodo-3-methyl-benzoic acid methyl ester (11.2 g) in dichloromethane (80 mL) was added dropwise over 25 minutes diisobutyl aluminium hydride (113 mL, 1.02 mol/L hexane solution) at −78° C., and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added dropwise methanol (10 mL) at the same temperature, and the mixture was stirred for 10 minutes. To the reaction mixture was added a saturated potassium sodium tartrate tetrahydrate aqueous solution (300 mL) under ice-cooling, and the mixture was stirred for 30 minutes. The reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was washed with hexane to give (5-fluoro-2-iodo-3-methyl-phenyl)methanol (7.15 g). To a suspension of the obtained compound (7.15 g) in chloroform (53 mL) and acetone (5.2 mL) was added manganese dioxide, and the mixture was stirred at room temperature for 4 hours. The reaction mixture was filtered through a Celite pad, and the filtrate was concentrated. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/n-hexane=0-15%) to give the title compound (3.54 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263622B2
Source datasetuspto-grants-2012_09
ORD IDord-e0ef9d5069ed4a78a26b304115f7c3b7
Source noteuspto-grants-2012_09