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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065633Generated: October 26, 2026

Triethylamine → 1-p-Phenylphenoxy-3,3-dimethyl-2-triethylsiloxy-1-(1,2,4-triazol-1-yl)-butane

https://huagongshe.com/reaction/1065633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorotriethylsilaneHCID 13819—
ReactantBitertanolHCID 91656—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product1-p-Phenylphenoxy-3,3-dimethyl-2-triethylsiloxy-1-(1,2,4-triazol-1-yl)-butaneHCID 2053955740.7%

Reaction Conditions

Temperature45 °C

Reaction Steps

5.5 g of 1-p-phenylphenoxy-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol is dissolved in 25 ml of THF. 2.9 g of triethylchlorosilane and 0.2 g of 4-dimethylaminopyridine are added under a nitrogen blanket. The mixture is heated to 45° C., and 3.3 g of triethylamine is added in portions. After the mixture has been stirred for 14 hours at from 40° to 50° C. it is cooled to room temperature, undissolved matter is filtered off, and the filtrate is concentrated. The product is further purified either by adding petroleum ether, followed by filtration and concentration, or by gel filtration (SiO2, CHCl3). There is obtained 3 g of 1-p-phenylphenoxy-3,3-dimethyl-2-triethylsiloxy-1-(1,2,4-triazol-1-yl)-butane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04330535
Source datasetuspto-grants-1982_05
ORD IDord-2f9a22956e5947f0a32bdb954971dfd7
Source noteuspto-grants-1982_05