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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426296Generated: October 31, 2026

Diethyl (cyanomethyl)phosphonate → (3-{[Tert-butyl(diphenyl)silyl]oxy}cyclobutylidene)acetonitrile

https://huagongshe.com/reaction/1426296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-((tert-Butyldiphenylsilyl)oxy)cyclobutanoneHCID 66824505—
SolventTetrahydrofuranHCID 8028—
Product(3-{[Tert-butyl(diphenyl)silyl]oxy}cyclobutylidene)acetonitrileHCID 66824450100.1%

Reaction Steps

To a solution of 1.0M potassium tert-butoxide in tetrahydrofuran (5.95 mL, 5.95 mmol) at 0° C. was added diethyl cyanomethylphosphonate (1.05 g, 5.95 mmol). The bath was removed and reaction allowed to warm to room temperature for 1 hour. The reaction was cooled to 0° C. and a solution of 3-{[tert-butyl(diphenyl)silyl]oxy}cyclobutanone (1.95 g, 6.01 mmol) in THF (10 mL) was added. Upon complete addition, the bath was removed and the reaction was allowed to warm to room temperature and stir overnight. The reaction solution was diluted with water and ethyl acetate. The aqueous layer was extracted with ethyl acetate three times. The combined extracts were washed with brine, dried over sodium sulfate, decanted and concentrated. The crude was purified silica gel column to give the desired product (2.07 g, 90%) as an oil. LCMS (M+H)+: 348.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933085B2
Source datasetuspto-grants-2015_01
ORD IDord-0461e984eb1b4f898fcd9469ba40a88f
Source noteuspto-grants-2015_01