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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588033Generated: November 1, 2026

2-Methyl-4-nitrophenol → HCID 66589491, compound

https://huagongshe.com/reaction/588033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitrophenolHCID 7442—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDimethylformamideHCID 6228—
ProductHCID 66589491HCID 6658949175%

Reaction Steps

A mixture of 2-methyl-4-nitrophenol (3.0 g, 19.6 mmol), TBS-Cl (3.0 g, 19.6 mmol), and TEA (2.2 g, 21.6 mmol) in DMF (30 mL) stirred at ambient temperature for 16 h. The mixture was partitioned between 10% aqueous sodium bicarbonate solution (100 mL) and ethyl acetate (100 mL), and the aqueous layer was extracted with ethyl acetate (100 mL). The combined organic layers were washed with 10% aqueous sodium bicarbonate (3×100 mL) and water (100 mL), and evaporated under vacuum. The residue was chromatographed in hexanes-ethyl acetate gradient, providing 3.9 g of tert-butyldimethyl(2-methyl-4-nitrophenoxy)silane, in 75% yield; 1H NMR (DMSO-d6) δ 0.29 (s, 6H), 1.00 (s, 9H), 2.24 (s, 3H), 7.03 (d, J=8.9 Hz, 1H), 8.02 (dd, J=2.8, 8.9 Hz, 1H), 8.12 (d, J=2.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227954B2
Source datasetuspto-grants-2016_01
ORD IDord-2b4da40cdaeb4b69b6da3c1df463db85
Source noteuspto-grants-2016_01