HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202262Generated: November 1, 2026
Dimethylformamide → trans-2-(2-(((Tert-butyldiphenylsilyl)oxy)methyl)cyclopropyl) acetonitrile
https://huagongshe.com/reaction/2202262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | trans-(2-(((Tert-butyldiphenylsilyl)oxy)methyl)cyclopropyl)methyl methanesulfonate | HCID 10025044 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans-2-(2-(((Tert-butyldiphenylsilyl)oxy)methyl)cyclopropyl) acetonitrile | HCID 131735738 | 94% |
Reaction Steps
A mixture of trans-(2-(((tert-butyldiphenylsilyl)oxy)methyl)cyclopropyl)methyl methanesulfonate (1.23 g, 2.94 mmol), potassium cyanide (0.383 g, 5.88 mmol) and DMF (10 mL) was stirred overnight at 60° C. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 10→60% ethyl acetate/hexane) to give trans-2-(2-(((tert-butyldiphenylsilyl)oxy)methyl)cyclopropyl)acetonitrile (0.970 g, 2.78 mmol, 94%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365520B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-7a7092ac1a1f423aa3bf29153142d695 |
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| Source note | uspto-grants-2016_06 |
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