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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256912Generated: October 26, 2026

Triethylamine → (1-benzyl-1H-pyrazol-4-yl)methoxy-tert-butyldimethylsilane

https://huagongshe.com/reaction/1256912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantSodium BicarbonateHCID 516892—
Reactant(1-benzyl-1H-pyrazol-4-yl)methanolHCID 16769828—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(1-benzyl-1H-pyrazol-4-yl)methoxy-tert-butyldimethylsilaneHCID 6850900997.2%

Reaction Steps

To a solution of (1-benzyl-1H-pyrazol-4-yl)methanol (3.84 g) in methylene chloride (100 mL) were added triethylamine (2.80 mL), 4-dimethylaminopyridine (100 mg) and tert-butyldimethylsilyl chloride (3.80 g) at room temperature, and the mixture was stirred for 2 hr. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture, and insoluble material was removed by filtration. Ethyl acetate (100 mL) was added to extract the filtrate, and the organic layer was washed with brine. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound (6.00 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461209B2
Source datasetuspto-grants-2013_06
ORD IDord-1dd59fc8675547669ea633f6b76cb4cc
Source noteuspto-grants-2013_06