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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975483Generated: October 30, 2026

Ammonium Chloride → 4-Hydroxy-2,3,5-trimethyl-alpha-[(trimethylsilyl)methyl]benzenemethanol

https://huagongshe.com/reaction/975483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
ReactantMagnesiumHCID 5462224—
Reactant4-Hydroxy-2,3,5-trimethylbenzaldehydeHCID 10899021—
SolventDiethyl EtherHCID 3283—
Product4-Hydroxy-2,3,5-trimethyl-alpha-[(trimethylsilyl)methyl]benzenemethanolHCID 19971959—

Reaction Conditions

Temperature0 °C

Reaction Steps

Mix magnesium turnings (240 mg, 10 mmol) and anhydrous ethyl ether under an inert atmosphere. Add a solution of chloromethyltrimethylsilane (1.9 g, 10 mmol) in anhydrous ethyl ether. Stir until the magnesium metal dissolves. Add a solution of 2,3,5-trimethyl-4-hydroxybenzaldehyde (1.7 g, 10 mmol) in anhydrous ethyl ether. Stir until reaction is complete. Cool the reaction mixture to 0° C. and add saturated ammonium chloride solution. Separate the ether layer, wash with water and dry (MgSO4). Evaporate to give 4-hydroxy-2,3,5-trimethyl-α-[(trimethylsilyl)methyl]benzenemethanol and purify by silica gel chromatrography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608095
Source datasetuspto-grants-1997_03
ORD IDord-7c3924ca28dc41a9a07aa01e0ef1519f
Source noteuspto-grants-1997_03