HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880243Generated: October 30, 2026
Trimethylsilyl cyanide → HCID 86761697, compound
https://huagongshe.com/reaction/1880243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | HCID 86761695 | HCID 86761695 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Product | HCID 86761697 | HCID 86761697 | — |
Reaction Steps
To a mixture of 0.83 g of 4-[5-[3,5-bis(trifluoromethyl)phenyl]-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]benzaldehyde and 0.36 g of trimethylsilylcyanide, 0.01 g of zinc iodide was added while stirring the mixture at 0° C. The resultant mixture was stirred at 60° C. for 10 minutes, and then left to be cooled down to room temperature. 2 mL of a 2M ammonia-methanol solution was added to the resultant reaction mixture, followed by continuing the stirring of the resultant reaction mixture at 50° C. further for 3.5 hours. After the completion of the reaction, the solvent was distilled off under reduced pressure and the resultant residue was purified by silica gel column chromatography eluting with ethyl acetate-hexane (1:2) to obtain 0.60 g of the objective substance as a brown resinoid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318757B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-0c0a74c2db7b467aaae41771da941a1b |
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| Source note | uspto-grants-2012_11 |
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