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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487195Generated: October 26, 2026

Triethylamine → 4-(3-((Tert-butyldimethylsilyloxy)methyl)-4-nitrophenyl)morpholine

https://huagongshe.com/reaction/1487195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(5-Morpholin-4-YL-2-nitro-phenyl)-methanolHCID 9878047—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-(3-((Tert-butyldimethylsilyloxy)methyl)-4-nitrophenyl)morpholineHCID 8669968590.9%

Reaction Steps

To a solution of (5-morpholino-2-nitrophenyl)methanol (3.0 g, 12.6 mmol), triethylamine (2.54 g, 25.2 mmol) and 4-dimethylaminopyridine (0.2 g) in dichloromethane (100 mL) was added tert-butylchlorodimethylsilane (2.83 g, 18.9 mmol). After the addition was over, the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate, and the organic phase was washed by saturated sodium bicarbonate, dried over anhydrous sodium sulfate, evaporated and purified by silica gel chromatography to afford the product 4-(3-((tert-butyldimethylsilyloxy)methyl)-4-nitrophenyl)morpholine (4.0 g, yield 90.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428508B2
Source datasetuspto-grants-2016_08
ORD IDord-ccaa05a926ba49a38405e9ef64798303
Source noteuspto-grants-2016_08