HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384563Generated: October 26, 2026
Allyl glycidyl ether → HCID 57772393, compound
https://huagongshe.com/reaction/384563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl glycidyl ether | HCID 7838 | — |
| Reactant | 1-(2-Trimethylsilylethyl)-1,1,3,3-tetramethyldisiloxane | HCID 58934338 | — |
| Product | HCID 57772393 | HCID 57772393 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367740B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-f597c0b270d44912b3897d9f57347efc |
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| Source note | uspto-grants-2013_02 |
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