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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625185Generated: November 2, 2026

Acetonitrile → HCID 11769906, compound

https://huagongshe.com/reaction/1625185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantMethanedione--ethanol (1/1)HCID 19604758—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 11769906HCID 1176990698.3%

Reaction Steps

To a reaction vessel was added acetonitrile (19.0 ml) and anhydrous THF (50 ml), cooled to −70° C. with dry ice/ethanol, then the solution of n-Butyl Lithium in n-hexane (2.5 M, 142.0 ml) was added dropwise slowly. After stirring for half an hour under this temperature, the solution of the compound II (44.6 g) in anhydrous THF (300 ml) was added dropwise slowly, and stirred for 1 h at the same temperature. The reaction is quenched by adding saturated aqueous ammonium chloride (700 ml), extracted with ethyl acetate (350 ml×3). The organic layers were combined, washed with saturated aqueous NaCl (350 ml), dried over anhydrous sodium sulfate, and concentrated to obtain the off-white title product (54.3 g). Yield: 98.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779199B2
Source datasetuspto-grants-2014_07
ORD IDord-de8e4ca7788743969c6d3b8d0d9e7253
Source noteuspto-grants-2014_07