HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417254Generated: October 30, 2026
Water → 4-(Tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyronitrile
https://huagongshe.com/reaction/417254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-(Tert-butyldimethylsilyloxy)-2,2-dimethylpropyl methanesulfonate | HCID 57439915 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(Tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyronitrile | HCID 10977213 | 57.6% |
Reaction Steps
To the solution of methanesulfonic acid 3-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-propyl ester (5 g, 16.8 mmol) in anhydrous dimethyl sulfoxide (50 mL) was added KCN (2.85 g, 44 mmol). The reaction mixture was heated at 120° C. for 16 h. The mixture was cooled, and water was added. The mixture was extracted with ethyl acetate twice. The combined organic layers were washed with saturated aqueous NaHCO3 solution, brine, dried over MgSO4, and concentrated. The residue was purified by chromatography (EtOAc:hexanes=1; 4) to give 4-(tert-butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyronitrile as a yellow oil (2.2 g, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088815B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-919875c044f24607bceace56d5a49ceb |
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| Source note | uspto-grants-2012_01 |
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