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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384564Generated: October 30, 2026

1-(2-Hydroxyethyl)piperazine → 1-(4-(2-Hydroxy-ethyl)-piperazin-1-yl)-3-(3-(1,1,3,3-tetramethyl-3-(2-trimethylsilanyl-ethyl)-disiloxanyl)-propoxy)-propan-2-ol

https://huagongshe.com/reaction/384564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
Reactant1,1,3,3-Tetramethyl-3-(3-oxiranylmethoxy-propyl)-1-(2-trimethylsilanyl-ethyl)-disiloxaneHCID 57772393—
SolventEthanolHCID 702—
Product1-(4-(2-Hydroxy-ethyl)-piperazin-1-yl)-3-(3-(1,1,3,3-tetramethyl-3-(2-trimethylsilanyl-ethyl)-disiloxanyl)-propoxy)-propan-2-olHCID 57772395—

Reaction Conditions

Temperature70 °C

Reaction Steps

2-piperazin-1-yl ethanol (0.74 g) and 20 mL of ethanol 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) 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367740B2
Source datasetuspto-grants-2013_02
ORD IDord-6f83c6bae4ff436a9bbe34e42b1f7ae5
Source noteuspto-grants-2013_02