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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821692Generated: November 1, 2026

Hydrochloric Acid → 1-(2-methoxyphenyl)-2-methylpropan-1-ol

https://huagongshe.com/reaction/1821692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant2-MethoxybenzaldehydeHCID 8658—
ReactantHCID 178418365HCID 178418365—
SolventWaterHCID 962—
Product1-(2-methoxyphenyl)-2-methylpropan-1-olHCID 22584774.8%

Reaction Steps

Dry tetrahydrofuran (3 mL) was added to 1.01 g (7.43 mmol) of commercially available 2-methoxybenzaldehyde under nitrogen atmosphere, and the mixture was ice-cooled. To the mixture was added dropwise a 3.8 mL (7.6 mmol) of tetrahydrofuran solution containing 2 mol/L isopropyl-magnesium bromide. After completion of dropwise addition, the reaction mixture was stirred in an ice bath for 1 hour. The reaction mixture was poured into water, made acidic with diluted hydrochloric acid, and then, extracted with ether. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed, and the obtained residue was purified by silica gel column chromatography (Wako gel C-100, hexane-ethyl acetate, gradient) to obtain 1.00 g (5.56 mmol, Yield: 74.8%) of 1-(2-methoxyphenyl)-2-methyl-1-propanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-a7aaae1ec6cb47e89448a1b9883226cf
Source noteuspto-grants-2009_10