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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721436Generated: November 3, 2026

Methanol → HCID 22414887, compound

https://huagongshe.com/reaction/1721436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzylamineHCID 7504—
ReactantSodium amideHCID 24533—
Reactant1-(benzyloxy)-2-bromo-4-methylbenzeneHCID 10731213—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22414887HCID 2241488772.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

100.0 g (2.56 mol) of sodium amide was added to 700 g (6.53 mol) of benzylamine under an argon atmosphere, and the mixture was stirred for 10 minutes at 60° C. A solution of 222.20 g (0.801 mol) of 1-benzyloxy-2-bromo-4-methylbenzene was dissolved in 400 ml of tetrahydrofuran was added dropwise to the above mixture over 50 minutes. The mixture was stirred for 50 minutes while maintaining the temperature at 60° C. Methanol was added under cooling with ice, and the mixture was poured into ice water. The reaction mixture was extracted with ethyl acetate-water, and the organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The residue obtained by evaporating the solvent was purified by column chromatography (silica gel, 10:1 mixture of n-hexane and ethyl acetate). The crude product thus obtained was recrystallized from n-hexane to obtain 175.80 g (yield: 72.3%) of the title compound as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510366
Source datasetuspto-grants-1996_04
ORD IDord-314e7fcbd1fb4391a79eae0406d46bbf
Source noteuspto-grants-1996_04