Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261469Generated: November 2, 2026

Ethanol → 1-(3-(Di(tert-butyldimethylsiloxy)-methyl-silanyl)-propoxy)-3-(2-(2-(2-hydroxy-ethoxy)-ethoxy)-ethylamino)-propan-2-ol

https://huagongshe.com/reaction/1261469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthanol, 2-[2-(2-aminoethoxy)ethoxy]-HCID 95875—
Reactant1,5-Di(tert-butyl)-3-(oxiranylmethylpropyl)-1,1,3,5,5-PentamethyltrisiloxaneHCID 86632280—
Product1-(3-(Di(tert-butyldimethylsiloxy)-methyl-silanyl)-propoxy)-3-(2-(2-(2-hydroxy-ethoxy)-ethoxy)-ethylamino)-propan-2-olHCID 57772565—

Reaction Conditions

Temperature70 °C

Reaction Steps

2-(2-(2-Amino-ethoxy)-ethoxy)-ethanol (3.52 g) and ethanol (40 mL) were charged to a 100 mL RB flask equipped with a magnetic stirrer. The mixture was stirred and heated to 70° C. 1,5-Di(tert-butyl)-3-(oxiranylmethylpropyl)-1,1,3,5,5-Pentamethyltrisiloxane (2.0 g) mixed with ethanol (10 mL) was placed in an addition funnel and added dropwise to the flask. The mixture was stirred and maintained at 70° C. for an additional 4 hours. Reaction progress was monitored by NMR spectroscopy. Upon reaction completion, the ethanol was removed by rotary evaporation, and the mixture was distilled under vacuum to remove impurities and excess raw material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470894B2
Source datasetuspto-grants-2013_06
ORD IDord-f9ff1826476d451ba05a45ceca9a0ba8
Source noteuspto-grants-2013_06