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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384565Generated: October 30, 2026

Diglycolamine → 1-(2-(2-Hydroxy-ethoxy)-ethylamino)-3-(3-(1,1,3,3-tetramethyl-3-(2-trimethylsilanyl-ethyl)-disiloxanyl)-propoxy)-propan-2-ol

https://huagongshe.com/reaction/384565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiglycolamineHCID 13578—
Reactant1,1,3,3-Tetramethyl-3-(3-oxiranylmethoxy-propyl)-1-(2-trimethylsilanyl-ethyl)-disiloxaneHCID 57772393—
SolventEthanolHCID 702—
Product1-(2-(2-Hydroxy-ethoxy)-ethylamino)-3-(3-(1,1,3,3-tetramethyl-3-(2-trimethylsilanyl-ethyl)-disiloxanyl)-propoxy)-propan-2-olHCID 57772397—

Reaction Conditions

Temperature70 °C

Reaction Steps

2-(2-Amino-ethoxy)-ethanol (3.02 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. 1,1,3,3-Tetramethyl-3-(3-oxiranylmethoxy-propyl)-1-(2-trimethylsilanyl-ethyl)-disiloxane (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. The reaction progress was monitored by NMR spectroscopy. Upon reaction completion, ethanol was removed under vacuum, and the mixture was vacuum distilled to remove impurities and excess raw material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367740B2
Source datasetuspto-grants-2013_02
ORD IDord-d8264dfca34646acb358c57894d2ed96
Source noteuspto-grants-2013_02