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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830209Generated: November 1, 2026

Ammonium Chloride → 1-(3,4,5,6-Tetramethoxy-2-methylphenyl)-1-(3-benzyloxyphenyl)methanol

https://huagongshe.com/reaction/1830209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
ReactantMagnesiumHCID 5462224—
Reactant2,3,4,5-Tetramethoxy-6-methylbenzaldehydeHCID 14852334—
SolventTetrahydrofuranHCID 8028—
Product1-(3,4,5,6-Tetramethoxy-2-methylphenyl)-1-(3-benzyloxyphenyl)methanolHCID 2205419095%

Reaction Steps

An anhydrous tetrahydrofuran (50 ml) solution of 3,4,5,6-tetramethoxy-2-methylbenzaldehyde (14 g, 0.058 mol) was added dropwise under ice cooling to a Grignard reagent (150 ml tetrahydrofuran solution) prepared from 3-(benzyloxy)bromobenzene (18.4 g, 0.070 mol) and magnesium (1.87 g, 0.077 mol), and the resulting solution was stirred for 2 hours. The reaction solution was poured in an aqueous solution of saturated ammonium chloride and extracted with ether. The extract was washed with saturated brine and then dried. The reaction solution was filtered, the filtrate was concentrated and the obtained crude product was purified by silica gel column chromatography (hexand:ethyl acetate=4:1) to obtain the titled compound (23.5 g, 0.055 mol, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064124B2
Source datasetuspto-grants-2006_06
ORD IDord-90161aa5746a4560a61d570802f2a027
Source noteuspto-grants-2006_06