HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966168Generated: November 1, 2026
Diethyl (cyanomethyl)phosphonate → (3-{[Tert-butyl(diphenyl)silyl]oxy}cyclobutylidene)acetonitrile
https://huagongshe.com/reaction/1966168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-((tert-Butyldiphenylsilyl)oxy)cyclobutanone | HCID 66824505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-{[Tert-butyl(diphenyl)silyl]oxy}cyclobutylidene)acetonitrile | HCID 66824450 | 74.7% |
Reaction Steps
To 1.0 M of potassium tert-butoxide in tetrahydrofuran (1.2 mL) was added dropwise, at 0° C., diethyl cyanomethylphosphonate (0.19 mL, 0.0012 mol). The reaction was warmed to rt and 30 min later cooled to 0° C. again. To the reaction mixture was added a solution of 3-[tert-butyl(diphenyl)silyl]oxycyclobutanone (0.25 g, 0.00077 mol) in THF (5 mL). The reaction was allowed to warm up to rt gradually and stirred at rt for 2 h. The reaction was quenched with saturated aq. NH4Cl, extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, concentrated. The resultant residue was purified with Combiflash (silica gel, 0-20% EtOAc/Hex) to give the desired product (0.2 g) as colorless oil. LCMS calculated for C22H26NOSi(M+H)+: 348.1 Found: 348.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420629B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-fbd77ee36538480bbd10a46ed8df84e0 |
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| Source note | uspto-grants-2013_04 |
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