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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384563Generated: October 26, 2026

Allyl glycidyl ether → HCID 57772393, compound

https://huagongshe.com/reaction/384563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl glycidyl etherHCID 7838—
Reactant1-(2-Trimethylsilylethyl)-1,1,3,3-tetramethyldisiloxaneHCID 58934338—
ProductHCID 57772393HCID 57772393—

Reaction Conditions

Temperature90 °C

Reaction Steps

1-(2-trimethylsilylethyl)-1,1,3,3-tetramethyldisiloxane (18.8 g) and chloroplatininc acid catalyst (ethanolic solution, 30 ppm Pt) were charged to a 100 ml round-bottomed (RB) flask equipped with a magnetic stirrer, reflux condenser, and N2 inlet. The mixture was stirred and heated to 90° C. 2-Allyloxymethyl-oxirane (10 g) was placed in an addition funnel and added dropwise to the flask. The mixture was stirred and maintained at 90° C. for an additional 4 hours. Reaction progress was followed by NMR spectroscopy. Upon reaction completion, excess 2-allyloxymethyl-oxirane was removed by vacuum distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367740B2
Source datasetuspto-grants-2013_02
ORD IDord-f597c0b270d44912b3897d9f57347efc
Source noteuspto-grants-2013_02